144891275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131271032-T-A

144891539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131271397-G-A

144891539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131271397-G-T

144891615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131271545-T-A

144891668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131271595-T-C

144891953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131271862-T-C

144892056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131271962-G-T

144892265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 131272168-C-G

144892265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 131272168-C-T

144892301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131272204-G-C

144892301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131272204-G-T

144892415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131272317-G-A

144892415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131272317-G-C

144892415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131272317-G-T

144892430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131272332-A-G

144892430-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131272332-A-T

144892488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131272417-G-C

144892498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131272425-C-T

144892524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131272455-G-C

144892559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131272490-A-G

144893593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131273682-T-C

144893628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131273730-T-C

144893629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131273731-G-A

144894541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131274659-G-A

144895506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131275519-G-C

144895566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131275572-G-A

144897167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 131277241-G-A

144897167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131277241-G-T

144897672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131277736-G-T

144897697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131277765-C-T

144898488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131279187-G-A

144898882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131279580-G-C

144898891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131279587-G-A

144899157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131279850-C-G

144899533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131280209-T-C

144899680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131280349-C-T

144899743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131280413-T-C

144899871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131280544-T-C

http://identifiers.org/hco/1/GRCh38#144899899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131280572-A-C

144900056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131280709-G-A

144900834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131281368-C-T

144900904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131281440-T-C

http://identifiers.org/hco/1/GRCh38#144900935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#131281471-C-A

144900955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131281482-C-T

144900969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131281496-C-T

144900986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131281513-A-G

144903095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131281724-G-T

http://identifiers.org/hco/1/GRCh38#144904059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131282585-C-A

144904105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131282638-C-T

144904132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131282661-T-G

144904282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131282806-A-T

144904348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131282874-G-T

144904735-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131282904-T-A

144904735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131282904-T-C

144904735-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131282904-T-G

144904984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131283138-G-A

144904984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131283138-G-C

144904984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131283138-G-T

http://identifiers.org/hco/1/GRCh38#144904989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#131283143-C-A

144905029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131283182-T-A

144905029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131283182-T-C

144905066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131283219-C-T

144905106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 131283264-T-C

144905199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131283357-C-G

144905199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 131283357-C-T

144905234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131283392-G-C

http://identifiers.org/hco/1/GRCh38#144905240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#131283398-C-A

144905240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131283398-C-T

144905266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131283435-G-A

144905266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131283435-G-T

144905267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131283436-G-A

144905267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131283436-G-C

144905267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131283436-G-T

144905289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131283458-G-A

144906098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131284657-C-G

144906098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131284657-C-T

144906109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131284668-C-T

144906171-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131284729-T-A

144906171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131284729-T-C

144906331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131284861-A-G

144906369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131284897-T-C

144906609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131284983-C-T

http://identifiers.org/hco/1/GRCh38#144906726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131285093-C-A

144906752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131285119-G-C

144907056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131285578-G-A

144908338-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131286694-T-A

144908338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131286694-T-C

144910179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131287205-G-A

144910263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131287288-T-C

144910449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131287473-T-A

144910449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131287473-T-C

144910883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131287921-G-A

144910883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131287921-G-T

144911011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131288048-G-A

144911322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131288652-C-G

144911325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131288653-G-T

144911769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131288922-C-G

http://identifiers.org/hco/1/GRCh38#144911912-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131289006-A-C

144911912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131289006-A-G

144911912-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131289006-A-T

144914024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131291150-C-T

144914240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131291312-C-G

144914407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131291472-G-A

144914476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131291541-G-A

http://identifiers.org/hco/1/GRCh38#144914675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131291723-C-A

144914675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131291723-C-G

http://identifiers.org/hco/1/GRCh38#144915062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131292093-C-A

144917389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131306038-G-A

144917676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131306332-T-G

144917747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131306407-A-G

144917806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131306460-G-A

144918021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 131306673-G-T

144918135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 131306787-C-T

http://identifiers.org/hco/1/GRCh38#144918244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131306892-C-A

144918244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 131306892-C-T

144918420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 131307070-C-T

144918424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 131307074-C-T

144919323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 131308140-C-T

144919554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 131308388-G-A

144921035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131309085-T-A

144921567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131309553-T-C

144923412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131312018-C-G

144923768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131312329-T-C

144924249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131312736-A-G

144927425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131314325-A-G

144928303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131315133-G-A

144928779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131315350-G-T

144928809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131315378-C-G

144928809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131315378-C-T

http://identifiers.org/hco/1/GRCh38#144928821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131315390-C-A

http://identifiers.org/hco/1/GRCh38#144928918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131315506-C-A

144928918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131315506-C-T

144929633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131316021-G-A

http://identifiers.org/hco/1/GRCh38#144929857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131316212-C-A

144929931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131316435-C-G

144930343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131316868-G-A

144930442-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131316958-T-A

144930483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131316999-C-T

144932185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131317965-G-A

144932766-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131321216-T-A

144932766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131321216-T-G

http://identifiers.org/hco/1/GRCh38#144932794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131321240-A-C

144932899-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131321341-T-A

144932901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131321343-C-T

144933697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131322090-T-C

144936393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 131323521-T-C

144936509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 131323625-G-A

144936509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 131323625-G-T

http://identifiers.org/hco/1/GRCh38#144936642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#131323750-C-A

144936758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131323868-A-G

144937452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131324470-A-G

144938594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131325457-C-T

144938611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131325483-C-T

http://identifiers.org/hco/1/GRCh38#144938675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131325586-A-C

144938675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131325586-A-G

144938683-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131325594-T-G

144938992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131325958-T-C

144939642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131326570-G-A

144939709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131326683-C-T

144939987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131326980-T-C

144940169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131327152-G-T

144940288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131327274-A-G

144940975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131327642-G-A

144941456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131328165-G-A

144941464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131328173-T-C

144941829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 131328624-C-T

144941895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 131328681-G-A

144942113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131328901-G-A

144942113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131328901-G-C

144942125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131328913-C-T

144942938-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131329401-A-T

144943106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131329547-T-A

144943106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131329547-T-C

144943111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131329552-G-A

144943630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131330017-G-A

http://identifiers.org/hco/1/GRCh38#144943635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131330022-A-C

144943820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131330328-T-A

144943889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131330385-T-C

144943954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131330451-G-A

144943954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131330451-G-T

http://identifiers.org/hco/1/GRCh38#144946128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131330997-C-A

http://identifiers.org/hco/1/GRCh38#144947313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131332407-C-A

144949145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131333935-G-T

144949149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131333939-C-G

144949168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131333958-C-T

144949237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131334027-A-G

http://identifiers.org/hco/1/GRCh38#144949663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131334746-C-A

http://identifiers.org/hco/1/GRCh38#144949943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131335013-C-A

144949943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131335013-C-T

http://identifiers.org/hco/1/GRCh38#144950122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131335273-C-A

144950292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131335439-G-C

144950370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131335518-G-C

144950370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131335518-G-T

144950484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131335632-T-C

144950751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131335834-G-A

144950775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131335857-T-A

144950781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131335863-T-C

144951802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131336164-T-C

144953151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131336703-C-T

144953209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131336750-G-A

144953280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131336822-A-G

144953376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131336906-G-A

144953537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131337052-T-C

144953979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131337834-C-T

144954114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131337969-C-T

144954303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131338145-T-G

144954341-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131338183-T-A

http://identifiers.org/hco/1/GRCh38#144954375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131338223-A-C

http://identifiers.org/hco/1/GRCh38#144954574-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131338824-A-C

144954731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131338976-G-A

144954738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131338983-A-G

144954921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131339150-T-C

144954989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131339216-G-A

144955015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131339239-A-G

144955163-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131339368-A-T

144955664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131339760-C-T

http://identifiers.org/hco/1/GRCh38#144955699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131339796-C-A

144955699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131339796-C-T

144955741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131339838-T-C

144956310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131341177-G-A

144956401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131341266-A-T

144959395-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131343159-C-G

144959395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131343159-C-T

http://identifiers.org/hco/1/GRCh38#144959517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131343292-C-A

144959517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131343292-C-T

144959536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131343311-G-A

144959897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131343802-G-C

144960006-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131343902-T-G

144960007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131343903-G-A

http://identifiers.org/hco/1/GRCh38#144960337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131344236-C-A

144960337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, splice_donor_variant
orthologous variants: 131344236-C-T

144960734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131344663-C-T

144960741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131344670-C-T

144960818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131344736-T-C

144960858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131344770-G-T

144961220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 131345121-C-T

144961281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 131345181-G-A

144961401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131345287-A-G

144961469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131345349-G-A

144961569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131345445-A-G

144961869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131345767-T-C

http://identifiers.org/hco/1/GRCh38#144962361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131346251-C-A

144962361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131346251-C-T

144963491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131346874-T-C

144963943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131347279-C-T

144964630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131347655-C-T

144970984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131347925-C-T

144971917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131348408-G-A

144971925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 131348416-C-T

144972374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131348864-G-T

144972402-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131348891-A-T

144972431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 131348913-T-C

144972570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131349034-G-A

144972570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131349034-G-T

144972880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131349277-G-A

144973153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131349499-A-G

144973153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131349499-A-T

144973867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131350164-G-A

144973867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131350164-G-C

http://identifiers.org/hco/1/GRCh38#144973879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131350176-C-A

144973879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131350176-C-T

144973988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131350258-C-T

144974115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131350392-G-A

http://identifiers.org/hco/1/GRCh38#144974359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131350622-C-A

144974539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131350798-A-G

144974613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131350861-G-A

144974613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131350861-G-T

144974751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131350953-C-T

144974958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131351122-G-C

144976459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131352327-A-G

144976596-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131352464-T-A

144976596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131352464-T-C

144976792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131352647-T-A

144976792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131352647-T-C

144977010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131352820-T-C

144977056-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131352865-A-T

144977070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131352881-A-G

144977272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131353070-A-G

http://identifiers.org/hco/1/GRCh38#144977278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131353076-A-C

144977361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131353358-A-T

144977366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131353363-A-G

144977402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 131353396-G-A

144977642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131353610-T-G

144977643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131353611-G-C

144977736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131353701-T-C

144977736-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131353701-T-G

144977895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 131353845-C-T

144977904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 131353854-G-A

144977942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 131353888-C-T

144978094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 131354024-G-A

144979005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131354604-T-A

144979005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131354604-T-G

144980344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131355383-T-A

144980486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 131355526-G-A

144980712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131355742-C-T

144980883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131355912-C-T

144981430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131356442-T-C

144981642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131356639-G-A

144982638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131356911-G-C

144982638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131356911-G-T

144982762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131357053-A-G

http://identifiers.org/hco/1/GRCh38#144982897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131357739-C-A

http://identifiers.org/hco/1/GRCh38#144983438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131358282-C-A

144985265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131358760-T-C

144985403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131358884-T-A

144985403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131358884-T-C

144985943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131359389-A-G

144985985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131359429-G-A

144986025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131359466-C-T

http://identifiers.org/hco/1/GRCh38#144986067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131359515-A-C

144986067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131359515-A-G

144986080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131359528-C-T

144986427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131359860-G-A

144986899-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131360517-T-A

144987174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131360759-T-C

144987179-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131360764-T-G

144987194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131360779-C-T

144987205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131360794-G-A

144987215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131360809-G-A

144987462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131361061-G-A

144987542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131361139-T-C

144988356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131361878-G-T

144989191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131363451-C-T

144989228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131363488-C-G

144989228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131363488-C-T

144989731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131363677-G-A

http://identifiers.org/hco/1/GRCh38#144994972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131364377-C-A

144994972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131364377-C-T

144995216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131364620-G-C

144995216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131364620-G-T

144995235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131364639-C-G

http://identifiers.org/hco/1/GRCh38#144995249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131364652-C-A

144995249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131364652-C-G

144995303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131364706-G-T

http://identifiers.org/hco/1/GRCh38#144995331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131364732-C-A

144995554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131364957-C-T

144995920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131365458-G-A

144996047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131365792-T-C

http://identifiers.org/hco/1/GRCh38#144997107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131366830-C-A

144997107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131366830-C-T

144997516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131366913-T-G

144998267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131368091-C-G

144998267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131368091-C-T

144998727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131368372-T-C

144998748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131368393-C-T

144998847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131368451-C-T

144999246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131368794-T-G

144999248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131368796-G-A

145001228-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131370940-T-A

http://identifiers.org/hco/1/GRCh38#145001346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131371057-C-A

145001497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131371210-A-T

145001542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131371257-C-T

http://identifiers.org/hco/1/GRCh38#145001633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131371351-C-A

145011494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131371600-C-G

145011602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131371703-A-G

145011718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131371800-C-T

145011822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131371914-C-G

145011847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131371939-C-G

145011851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131371943-G-A

145011932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131372035-A-G

http://identifiers.org/hco/1/GRCh38#145011933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131372036-C-A

http://identifiers.org/hco/1/GRCh38#145012335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131372490-C-A

145012435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131372773-A-G

http://identifiers.org/hco/1/GRCh38#145015497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131373784-C-A

145015516-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131373800-T-A

145015585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131373854-T-C

145015682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131373950-C-T

145016126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131374368-G-A

145016546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131374693-C-G

145016644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131374806-G-A

145016775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131374939-T-C

145017221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131375392-C-T

145017369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131375491-G-C

145017759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131376054-C-T

145017848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131376143-C-T

145018259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131377263-G-A

145019624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131378680-G-T

145019630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131378686-A-T

145019963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 131379026-G-A

145019964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 131379027-G-A

http://identifiers.org/hco/1/GRCh38#145021124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131379453-C-A

145021373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131380380-A-T

http://identifiers.org/hco/1/GRCh38#145021420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131380413-C-A

http://identifiers.org/hco/1/GRCh38#145021928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131380645-C-A

145022158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131380850-A-G

http://identifiers.org/hco/1/GRCh38#145022217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131380910-C-A

145022217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131380910-C-T

http://identifiers.org/hco/1/GRCh38#145022250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131380946-C-A

145022524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131381170-G-C

145022524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131381170-G-T

145022726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131381369-C-T

145025671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131382018-C-T

145025757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131382087-T-C

http://identifiers.org/hco/1/GRCh38#145026734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131383257-A-C

145026851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131383371-C-T

145028196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131384521-A-G

145028230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131384543-C-T

145034094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131386571-C-T

145034280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131386669-G-T

145034385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131386764-A-G

http://identifiers.org/hco/1/GRCh38#145034947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131387276-C-A

http://identifiers.org/hco/1/GRCh38#145035894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131388651-C-A

145036023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 131388802-C-T

http://identifiers.org/hco/1/GRCh38#145036492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131389260-C-A

145036492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131389260-C-T

http://identifiers.org/hco/1/GRCh38#145036534-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131389291-A-C

145036716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131389654-T-C

145037110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131390057-C-T

145037386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131390336-G-A

145037412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131390362-T-C

http://identifiers.org/hco/1/GRCh38#145038082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131391021-A-C

145038621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131391600-C-T

145038852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131391792-G-C

145039530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131392408-G-A

145039530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131392408-G-T

145040342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131393402-A-T

145040460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131393520-T-C

http://identifiers.org/hco/1/GRCh38#145040475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131393535-A-C

http://identifiers.org/hco/1/GRCh38#145040567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131393626-A-C

http://identifiers.org/hco/1/GRCh38#145040673-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131393733-A-C

145040766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131393821-T-C

145040779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131393833-C-T

http://identifiers.org/hco/1/GRCh38#145040883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131393930-C-A

145040883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131393930-C-T

145040970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131393990-C-T

145041034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131394051-C-T

145041064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131394070-G-A

145041064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131394070-G-C

145041064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131394070-G-T

145041801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 131394353-C-T

145041887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131394418-G-A

145042257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131394629-T-C

http://identifiers.org/hco/1/GRCh38#145042369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131394755-A-C

145042390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131394777-C-T

145042562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131394934-G-A

145042562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131394934-G-T

145043117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131395452-G-A

145043117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131395452-G-T

145043584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131395899-C-T

145043889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131396173-T-C

145044157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131396555-G-A

145044396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131396863-G-A

145044406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131396874-T-A

145044473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131396938-G-A

145044478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131396943-G-T

145044783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 131398251-A-G

145044806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 131398275-T-A

145044987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131398411-G-T

145045007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131398431-G-A

145045756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131399399-C-T

http://identifiers.org/hco/1/GRCh38#145046028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131399618-C-A

145046158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131399747-T-C

145046834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131400481-G-A

http://identifiers.org/hco/1/GRCh38#145047743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131401069-C-A

145048392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131401712-G-T

http://identifiers.org/hco/1/GRCh38#145048477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131401797-C-A

145048507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131401827-G-T

145048514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131401834-T-C

145048687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131401992-G-C

145048693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131401998-C-T

145048707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131402012-G-C

http://identifiers.org/hco/1/GRCh38#145050847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131403983-C-A

145050847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131403983-C-T

http://identifiers.org/hco/1/GRCh38#145050912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131404046-C-A

145050944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131404078-G-A

145051144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131405662-C-T

http://identifiers.org/hco/1/GRCh38#145051434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131405997-C-A

145051434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131405997-C-G

145051434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131405997-C-T

145051462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131406025-G-T

145051464-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131406027-A-T

145051555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131406091-G-A

145051671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131406189-C-T

145051679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131406197-T-C

145055647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131410419-C-G

145056040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131411040-T-C

145056439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131411636-T-G

145056546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131411736-C-T

145056784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131411944-G-A

145057201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131412701-C-T

145057234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131414651-T-A

145057369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131414789-T-C

145057488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131414907-T-G

145057492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131414911-G-T

145058153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131415235-G-A

145058153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131415235-G-C

145058472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131416055-A-G

145058490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131416073-G-A

http://identifiers.org/hco/1/GRCh38#145058588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131416172-A-C

145058588-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131416172-A-T

145059011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131416278-T-G

145059021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131416286-T-C

145059021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131416286-T-G

145060101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131417334-C-T

145060214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131417451-G-T

145061060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131418189-G-C

145062163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131419026-G-A

145062223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131419070-C-G

145062223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131419070-C-T

145062228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131419075-G-A

145062521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131419330-C-T

145062583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131419391-C-T

145062645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 131419450-C-T

http://identifiers.org/hco/1/GRCh38#145062678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131419483-A-C

145062678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 131419483-A-T

145063146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131419951-T-C

145063569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131420385-G-C

145063879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131420724-T-C

145063895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131420741-C-G

145063895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131420741-C-T

http://identifiers.org/hco/1/GRCh38#145063899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131420745-C-A

145063899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131420745-C-T

145064237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131421179-G-A

145064636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131421563-C-T

http://identifiers.org/hco/1/GRCh38#145064811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131421711-C-A

145065592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131422439-C-G

145065637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131422484-C-T

145065760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131422597-A-G

145067778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131424868-G-A

http://identifiers.org/hco/1/GRCh38#145067888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131424985-C-A

145067888-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131424985-C-G

145067904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131425001-G-A

http://identifiers.org/hco/1/GRCh38#145068228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131427068-C-A

145068328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131427160-T-C

145068342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131427182-G-C

145068368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131427208-A-G

145068415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131427420-C-T

145068437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131427445-T-C

145068623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131427638-C-T

145068718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131427735-T-C

145068732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131427749-C-T

145068769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131427772-A-G

145068786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131427789-C-G

145069236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131429154-G-A

145069272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131429193-C-T

145069388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131429306-G-C

145069601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131429522-C-T

145069794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131429742-T-C

http://identifiers.org/hco/1/GRCh38#145069860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131429836-C-A

145069953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131429940-T-C

145070071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131430060-C-G

145070197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131430202-C-G

145070233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131430234-G-A

145070513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131430512-G-T

145071308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131431782-C-T

145071337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131431811-T-G

145071348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131431822-A-G

145071441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131431908-C-G

145071441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131431908-C-T

145071579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131431984-T-C

145072536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131432938-G-A

145072627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131433042-G-T

145072711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131433126-A-G

145072718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131433133-C-T

http://identifiers.org/hco/1/GRCh38#145073014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131433420-C-A

145073469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131433834-C-G

145074150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131434414-T-A

145076690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131438440-G-A

145076710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131438460-A-G

145076929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131438672-A-G

145078892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131440034-C-T

145078975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131440282-C-T

145079620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131440854-G-A

145081226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131441736-G-A

145081574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131441893-G-T

145081706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131442050-G-A

145081745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131442063-T-A

145081745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131442063-T-C

145081745-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131442063-T-G

145081989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131442304-A-G

145082064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131442421-A-G

145082364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131442698-C-G

145082364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131442698-C-T

145082365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131442699-G-A

145082750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131443267-G-C

145082844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131443357-G-C

145083312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131443698-G-C

145083409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131443795-T-A

145083412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131443798-G-A

145084326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131444811-G-A

145084663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131445146-T-A

145084763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131445247-C-G

145084783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131445267-G-A

145084887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131445363-C-T

145086591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131446395-A-T

145086618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131446413-G-C

http://identifiers.org/hco/1/GRCh38#145086641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131446429-C-A

145086680-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131446473-T-A

145086693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131446486-A-G

145086694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131446487-A-G

145086703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131446496-A-G

145087259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131447246-T-A

http://identifiers.org/hco/1/GRCh38#145087301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131447275-A-C

http://identifiers.org/hco/1/GRCh38#145087506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131447463-C-A

145087887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131447797-C-T

145088154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131448004-G-T

145088315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131448165-C-T

145088468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131448462-G-A

145088489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131448469-G-A

145088679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131448641-T-C

http://identifiers.org/hco/1/GRCh38#145088702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131448664-C-A

145088724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131448684-T-C

http://identifiers.org/hco/1/GRCh38#145088737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131448695-C-A

145089368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131448987-C-T

145090170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131449921-C-G

145090232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131450125-C-G

145090232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131450125-C-T

145091179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131451030-T-A

145091179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131451030-T-C

145091378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 131451216-A-G

145091937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131451787-G-T

145092012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 131451867-G-A

145092948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 131452789-C-T

145094524-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131454328-T-G

145094752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131454549-G-A

145095095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131454845-G-A

http://identifiers.org/hco/1/GRCh38#145095145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#131454896-C-A

145095154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35237
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131454905-G-A