GRCh38/hg38 17p13.1(chr17:7478195-8435524)x1 Detail (hg19) (ALOX12B, ALOX15B, ATP1B2, CD68, CHD3, EFNB3, EIF4A1, GUCY2D, PER1, PFAS, POLR2A, RPL26, SHBG, SOX15, VAMP2, TP53, TRG-GCC2-6, TRK-TTT3-5, TRL-TAG1-1, TRQ-CTG1-5, TRR-TCT2-1, TNFSF13, TNFSF12, KCNAB3, AURKB, FXR2, MPDU1, ARHGEF15, KDM6B, SENP3, SNORA67, RANGRF, BORCS6, WRAP53, ZBTB4, TRAPPC1, ALOXE3, CTC1, NDEL1, TMEM107, NAA38, HES7, TMEM88, SAT2, CNTROB, CYB5D1, KRBA2, DNAH2, ODF4, RNF227, LINC00324, SLC25A35, TNFSF12-TNFSF13, SLC35G6, RNF222, SNORA48, SNORD10, SCARNA21, SNORD118, LOC100128288, TRS-CGA1-1, TRW-CCA3-3, TRW-CCA1-1, TRP-CGG1-3, TRS-AGA2-6, TRT-AGT1-1, TRG-TCC3-1, TRT-AGT1-2, TRS-GCT4-3, TRD-GTC2-11, TRI-AAT5-5, TRI-AAT4-1, TRT-AGT5-1, MIR4314, SENP3-EIF4A1, MIR4521, MPDU1-AS1, MIR6883, LOC105371520, LOC106794092, LOC111828490, LOC112533665, LOC112533683, LOC116276454, LOC121587574, LOC121587575, LOC124904106, LOC126862481, LOC126862482, LOC126862483, LOC126862484, LOC126862485, LOC129390831, LOC129390832, LOC130060148, LOC130060149, LOC130060150, LOC130060151, LOC130060152, LOC130060153, LOC130060154, LOC130060155, LOC130060156, LOC130060157, LOC130060158, LOC130060159, LOC130060160, LOC130060161, LOC130060162, LOC130060163, LOC130060164, LOC130060165, LOC130060166, LOC130060167, LOC130060168, LOC130060169, LOC130060170, LOC130060171, LOC130060172, LOC130060173, LOC130060174, LOC130060175, LOC130060176, LOC130060177, LOC130060178, LOC130060179, LOC130060180, LOC130060181, LOC130060182, LOC130060183, LOC130060184, LOC130060185, LOC130060186, LOC130060187, LOC130060188, LOC130060189, LOC130060190, LOC130060191, LOC130060192, LOC130060193, LOC130060194, LOC130060195, LOC130060196, LOC130060197, LOC130060198, LOC130060199, LOC130060200, LOC130060201, LOC130060202, LOC130060203, LOC130060204, LOC130060205, LOC130060206, LOC130060207, LOC130060208, LOC130060209, LOC130060210, LOC130060211, LOC130060212, LOC130060213, LOC130060214, LOC130060215, LOC130060216, LOC130060217, LOC130060218, LOC130060219, LOC130060220, LOC130060221, LOC130060222, LOC130060223, LOC130060224, LOC130060225, LOC130060226, LOC130060227, LOC130060228, LOC130060229, LOC130060230, LOC130060231, LOC130060232, LOC130060233, LOC130060234, LOC130060235, LOC130060236, LOC130060237, LOC130060238, LOC130060239, LOC130060240, LOC130060241, LOC130060242, LOC130060243, LOC130060244, LOC130060245, LOC130060246)

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Information

Genome

Assembly	Position
hg19	chr17:7,381,514-8,338,842
hg38	chr17:7,478,195-8,435,524 View the variant detail on this assembly version.

Summary

Links

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Pathogenic	2011-08-12	criteria provided, single submitter		not provided	Detail

CIViC

[No Data.]

DisGeNET

[No Data.]

Annotation

Descrption	Source	Links
GRCh38/hg38 17p13.1(chr17:7478195-8435524)x1 AND See cases	ClinVar	Detail

Gene	Transcript ID	Exon Number	Chromosome	Start	Stop	Type	Amino Mutation	Transcript Position	Links

Gene	Transcript ID	Chromosome	Start	Stop	Links

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