http://identifiers.org/hco/8/GRCh38#144529233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76608239-C-A

144529233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: 3 prime UTR variant
orthologous variants: 76608239-C-T

144529307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: 3 prime UTR variant
orthologous variants: 76608290-G-C

144529307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: 3 prime UTR variant
orthologous variants: 76608290-G-T

144529313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: 3 prime UTR variant
orthologous variants: 76608296-G-A

144529313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: 3 prime UTR variant
orthologous variants: 76608296-G-T

144529880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: 3 prime UTR variant
orthologous variants: 76608749-C-G

144529880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: 3 prime UTR variant
orthologous variants: 76608749-C-T

http://identifiers.org/hco/8/GRCh38#144530173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#76609014-C-A

144530173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 76609014-C-G

144530173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 76609014-C-T

144530245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: 3 prime UTR variant
orthologous variants: 76609068-G-T

144530272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: 3 prime UTR variant
orthologous variants: 76609075-C-T

144530275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: 3 prime UTR variant
orthologous variants: 76609078-G-A

144530275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: 3 prime UTR variant
orthologous variants: 76609078-G-T

144530590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76609350-C-G

144530590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76609350-C-T

144530972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76609788-A-G

144530972-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76609788-A-T

144531164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76609988-C-T

144532437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76610259-G-T

http://identifiers.org/hco/8/GRCh38#144532525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76610307-A-C

144532525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76610307-A-T

144532752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76610455-G-A

144532761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76610471-G-A

144532842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76610603-T-A

144532842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76610603-T-C

144533029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76610736-C-T

http://identifiers.org/hco/8/GRCh38#144533362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76611073-C-A

144533362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76611073-C-T

http://identifiers.org/hco/8/GRCh38#144533472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76611110-C-A

144533472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76611110-C-T

http://identifiers.org/hco/8/GRCh38#144533986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76611494-C-A

144533986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76611494-C-T

144534009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76611511-C-G

144534084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76611567-C-G

http://identifiers.org/hco/8/GRCh38#144534118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76611592-C-A

144534118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76611592-C-T

144534206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 76611680-G-A

144534206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 76611680-G-C

144534206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 76611680-G-T

http://identifiers.org/hco/8/GRCh38#144534318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76611759-C-A

144534318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76611759-C-G

144534318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76611759-C-T

144534775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76612226-C-G

144535236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76612568-C-T

144535366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76612705-T-C

144535703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76612946-G-A

http://identifiers.org/hco/8/GRCh38#144535862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76613081-A-C

144536002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76613193-G-A

144536229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76613347-G-C

144536294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76613389-G-A

144536294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76613389-G-C

144536584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76613619-G-A

144536737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76613709-C-G

144536782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76613751-C-G

http://identifiers.org/hco/8/GRCh38#144537005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76613940-C-A

http://identifiers.org/hco/8/GRCh38#144537552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76614399-C-A

144537629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76614483-G-A

144537629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76614483-G-C

144537629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76614483-G-T

144537679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76614528-T-C

144537945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76614787-A-G

144538379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76615117-G-A

144538379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76615117-G-C

http://identifiers.org/hco/8/GRCh38#144538387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76615125-C-A

144543236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76617341-G-C

144543240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76617345-T-G

144543407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76617455-G-C

144543413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76617461-A-T

144543751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76617735-A-G

144543805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76617771-G-A

144543805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76617771-G-T

http://identifiers.org/hco/8/GRCh38#144543825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76617789-C-A

144543887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76617839-A-G

144543928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76617887-A-G

144544016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76617969-G-A

144544016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76617969-G-T

144544039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76617989-T-C

144544062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76618026-T-C

http://identifiers.org/hco/8/GRCh38#144544254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76618213-C-A

144544755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76618668-G-A

144544981-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76618853-T-G

144544998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76618870-C-T

144545104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76618939-G-A

144545104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76618939-G-C

144545104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76618939-G-T

144545149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76618961-G-A

144545149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76618961-G-T

144545178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76618988-C-G

144545178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76618988-C-T

144545203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76619014-C-T

144545259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76619087-A-G

144545415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76619243-G-A

144545415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 76619243-G-C

144545415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 76619243-G-T

144545556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76619384-G-A

http://identifiers.org/hco/8/GRCh38#144545884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76619711-C-A

144545884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76619711-C-G

http://identifiers.org/hco/8/GRCh38#144545920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76619729-C-A

144545920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76619729-C-T

http://identifiers.org/hco/8/GRCh38#144545943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76619750-C-A

144545943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76619750-C-T

144546071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76619837-T-C

http://identifiers.org/hco/8/GRCh38#144546180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76619943-A-C

144546271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76619994-G-A

144546274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76619997-C-T

http://identifiers.org/hco/8/GRCh38#144546450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76620130-C-A

144546451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76620131-C-T

144546575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76620181-G-A

144547053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76620584-C-T

http://identifiers.org/hco/8/GRCh38#144547089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76620609-C-A

144547089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76620609-C-G

144547089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76620609-C-T

http://identifiers.org/hco/8/GRCh38#144547112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76620641-C-A

144547112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76620641-C-T

144547241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76620770-C-T

144547309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76620838-G-A

144547309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: missense variant
orthologous variants: 76620838-G-C

http://identifiers.org/hco/8/GRCh38#144547397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76620926-C-A

144547397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76620926-C-G

144547397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76620926-C-T

http://identifiers.org/hco/8/GRCh38#144547508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76621028-C-A

144547508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76621028-C-T

http://identifiers.org/hco/8/GRCh38#144547513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/15/GRCm39#76621033-C-A

144547513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: missense variant
orthologous variants: 76621033-C-T

144547542-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: missense variant
orthologous variants: 76621062-T-A

144547542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: missense variant
orthologous variants: 76621062-T-C

http://identifiers.org/hco/8/GRCh38#144547592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76621112-C-A

144547592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: missense variant
orthologous variants: 76621112-C-G

144547610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76621130-G-A

144547610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76621130-G-C

144547610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76621130-G-T

http://identifiers.org/hco/8/GRCh38#144547619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76621139-C-A

144547619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76621139-C-G

144547619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76621139-C-T

144547631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76621151-T-C

http://identifiers.org/hco/8/GRCh38#144547640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76621160-C-A

144547640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76621160-C-G

144547640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76621160-C-T

http://identifiers.org/hco/8/GRCh38#144547724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76621244-A-C

144547724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76621244-A-G

144547817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76621337-G-A

144547817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76621337-G-C

144547817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76621337-G-T

144548093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76621613-G-A

144548093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: missense variant
orthologous variants: 76621613-G-T

144548183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76621703-G-A

144548183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76621703-G-T

144548288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76621808-G-A

144548351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76621871-G-T

144548432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76621952-A-G

144548432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76621952-A-T

144548497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 76622017-G-A

144548497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 76622017-G-T

144548504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76622024-G-A

144548504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76622024-G-T

144554223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76624687-C-T

144554591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76625048-G-A

http://identifiers.org/hco/8/GRCh38#144554998-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76625355-A-C

144555165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76625415-A-T

144555212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76625437-G-A

144555307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76625529-G-A

144555580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76625733-G-A

http://identifiers.org/hco/8/GRCh38#144555740-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76625879-A-C

144555740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76625879-A-G

144555812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76626099-C-T

144577279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76634846-C-T

http://identifiers.org/hco/8/GRCh38#144577296-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76634867-A-C

http://identifiers.org/hco/8/GRCh38#144580775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76635682-C-A

144580775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76635682-C-T

http://identifiers.org/hco/8/GRCh38#144580778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76635685-C-A

http://identifiers.org/hco/8/GRCh38#144580893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76635775-C-A

144580950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76635829-G-T

144581047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: missense variant
orthologous variants: 76635917-G-T

144581106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76635976-A-G

144581106-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: missense variant
orthologous variants: 76635976-A-T

144581163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76636033-G-A

144581163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: missense variant
orthologous variants: 76636033-G-T

http://identifiers.org/hco/8/GRCh38#144581170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76636040-C-A

144581170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: missense variant
orthologous variants: 76636040-C-T

144581214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76636084-G-A

144581214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76636084-G-C

144581241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76636111-G-A

144581241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76636111-G-C

144581241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76636111-G-T

144581247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76636117-G-A

144581247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76636117-G-T

http://identifiers.org/hco/8/GRCh38#144581289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76636158-C-A

144581289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76636158-C-G

144581289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76636158-C-T

144584102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76637006-T-A

144584102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76637006-T-C

144589740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76645493-C-T

144589940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76645679-A-T

144589954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76645694-C-T

144589969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76645708-G-A

144590038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76645797-C-G

144592232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76647126-G-A

144604411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76648669-G-A

144604518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76648761-T-C

144604806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76649136-T-C

144605246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76649500-G-A

144605316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76649521-C-T

http://identifiers.org/hco/8/GRCh38#144605422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76649582-C-A

144605422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76649582-C-T

144605423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76649583-G-A

144605423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76649583-G-T

144605513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76649661-C-T

144605543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: synonymous variant
orthologous variants: 76649693-C-T

144605639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: 5 prime UTR variant
orthologous variants: 76649792-G-A

http://identifiers.org/hco/8/GRCh38#144615743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: -C-A

144619249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: -C-G

144677359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76695948-G-A

http://identifiers.org/hco/8/GRCh38#144680653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76698473-C-A

144680714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76698531-C-T

144680903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76698946-A-G

144681201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76699221-C-T

144681250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76699266-G-A

144681257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76699273-A-G

144683896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76700721-T-C

http://identifiers.org/hco/8/GRCh38#144684186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76700997-C-A

http://identifiers.org/hco/8/GRCh38#144684188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76700999-C-A

144684243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76701034-G-T

144684988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76701675-G-C

144685123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76701799-T-C

144685577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76702097-G-A

144685702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76702208-G-C

http://identifiers.org/hco/8/GRCh38#144685913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#76702399-A-C

144685995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76702472-G-A

http://identifiers.org/hco/8/GRCh38#144686049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#76702516-C-A

144686049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76702516-C-T

144686051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76702518-A-G

144686344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76702764-C-T

144686377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29351
most severe consequence: intron variant
orthologous variants: 76702797-G-A