101915044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8134418-G-A

101915044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8134418-G-C

101915044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8134418-G-T

101915176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8134292-G-A

http://identifiers.org/hco/11/GRCh38#101915187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8134281-A-C

101915224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8134246-A-G

101915238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8134232-T-C

101915238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8134232-T-G

101915267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8134227-G-A

http://identifiers.org/hco/11/GRCh38#101915373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#8134136-C-A

101915373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 8134136-C-T

101915374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 8134135-T-A

101915387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 8134122-G-A

101915387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 8134122-G-C

101915399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 8134110-C-G

http://identifiers.org/hco/11/GRCh38#101915534-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#8134025-A-C

101915534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 8134025-A-G

http://identifiers.org/hco/11/GRCh38#101915923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8133652-C-A

101915923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8133652-C-T

101915954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8133630-G-T

101915956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8133628-G-A

101915956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8133628-G-C

101915956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8133628-G-T

101915958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8133626-A-G

101915958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8133626-A-T

101915984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8133601-A-G

101915984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8133601-A-T

101916070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8133518-T-G

101916158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8133431-G-A

101916158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8133431-G-T

101916384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 8133230-G-T

http://identifiers.org/hco/11/GRCh38#101916449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8133176-C-A

101919435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8132323-T-G

101920060-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8131761-T-G

101920335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8131450-T-C

101920593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8131260-T-A

http://identifiers.org/hco/11/GRCh38#101920626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8131239-C-A

101920626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8131239-C-T

101921039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8130940-C-T

101921167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8130831-A-G

101921284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8130742-C-T

101921358-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8130679-T-G

101921407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8130629-C-G

101922567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8130380-A-G

http://identifiers.org/hco/11/GRCh38#101922750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8130205-C-A

101922750-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 8130205-C-G

101922750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 8130205-C-T

101922766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8130189-T-C

101923655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8129251-T-C

101931065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8124567-C-T

101931588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8124085-T-G

101931822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8123880-G-A

101931867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8123839-A-T

101931954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8123755-G-T

101932059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8123654-A-G

101932225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8123483-T-C

101932296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8123412-T-C

101932321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8123383-C-T

101932577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8123154-C-T

101932654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8123073-T-C

http://identifiers.org/hco/11/GRCh38#101943552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8121603-A-C

101943964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8121076-A-G

101944184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8120877-T-C

101944198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8120862-G-A

101944198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8120862-G-T

101944233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8120818-T-C

101944248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8120803-T-C

101944533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8120519-T-C

101944909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8114482-A-G

101945225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8114190-T-C

101945236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8114180-G-A

101945255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8114164-T-C

101945274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8114145-A-G

101945411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8113989-A-G

http://identifiers.org/hco/11/GRCh38#101945586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8113826-C-A

101945633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8113785-G-A

101945796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8113626-G-A

101945917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8113514-A-G

101946949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8113196-T-A

101946949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8113196-T-C

101946996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8113156-C-T

101947055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8113090-G-A

101947161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8112984-A-G

101947198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8112949-T-C

101947413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8112761-T-C

101947454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8112722-A-G

101947454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8112722-A-T

101947530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8112651-C-G

101947778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8112440-A-G

101947897-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8112321-A-T

101947914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8112304-T-C

http://identifiers.org/hco/11/GRCh38#101947993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8112237-A-C

101947993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8112237-A-G

101947993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8112237-A-T

101948001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8112229-T-C

101948122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 8112099-T-C

101948149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 8112072-A-G

101948156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8112065-G-T

101948203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8111945-T-C

http://identifiers.org/hco/11/GRCh38#101948232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8111907-C-A

http://identifiers.org/hco/11/GRCh38#101948238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8111901-C-A

101948238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8111901-C-T

101948621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8111295-T-C

101948758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8110998-T-C

101948772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8110943-C-T

101948816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8110883-A-G

101949003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8110640-C-G

101949003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8110640-C-T

101952344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8108682-C-T

101952922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8107994-G-A

101953300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8107734-A-G

101954452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8107015-G-A

http://identifiers.org/hco/11/GRCh38#101954484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8106987-C-A

101954569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8106878-C-G

101954834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8106644-T-G

101955022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8106421-T-C

101955435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8106069-C-T

101955715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8105860-C-T

101955846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 8105733-A-G

101955850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 8105729-T-C

http://identifiers.org/hco/11/GRCh38#101956114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8105474-C-A

101956114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 8105474-C-T

http://identifiers.org/hco/11/GRCh38#101956130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8105458-C-A

101956132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 8105456-C-G

101956135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 8105453-A-G

http://identifiers.org/hco/11/GRCh38#101956285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8105303-C-A

101956285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 8105303-C-G

101956285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 8105303-C-T

101956442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 8105152-C-T

101956474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 8105120-C-G

101956547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 8105047-C-T

101956552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 8105042-T-A

101956686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 8104908-A-G

101956779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 8104818-C-T

http://identifiers.org/hco/11/GRCh38#101956793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8104804-C-A

101957036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8104570-A-G

101957037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8104569-A-T

101957054-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8104552-A-T

101957386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8104241-C-G

101957386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8104241-C-T

101957746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8103884-G-T

101957951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8103704-A-G

http://identifiers.org/hco/11/GRCh38#101958041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8103638-C-A

101958041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8103638-C-T

http://identifiers.org/hco/11/GRCh38#101958085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8103596-C-A

101958085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8103596-C-T

101958433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8103263-T-C

101958433-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8103263-T-G

101961451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8102085-T-C

101961451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8102085-T-G

101961622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8101936-T-C

http://identifiers.org/hco/11/GRCh38#101961712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8101875-C-A

101961735-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 8101852-T-A

101961735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 8101852-T-C

http://identifiers.org/hco/11/GRCh38#101961996-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8101585-A-C

101962011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 8101570-G-A

http://identifiers.org/hco/11/GRCh38#101962036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8101545-C-A

101962036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 8101545-C-T

101962158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 8101423-C-T

http://identifiers.org/hco/11/GRCh38#101962205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8101376-C-A

101962216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 8101365-C-T

101962236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 8101345-G-A

101962251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 8101330-A-G

101962278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 8101303-T-G

101962297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 8101284-A-G

101962303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 8101278-C-T

101962375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 8101206-A-G

101962407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 8101174-C-T

101962476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 8101120-C-T

http://identifiers.org/hco/11/GRCh38#101962908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8100685-A-C

101962908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 8100685-A-G

101963136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 8100460-T-C

http://identifiers.org/hco/11/GRCh38#101963243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8100353-C-A

101963243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 8100353-C-T

101963387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 8100212-A-G

101963694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 8099905-G-A

http://identifiers.org/hco/11/GRCh38#101963725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8099883-C-A

101963764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 8099844-G-C

101963796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 8099812-G-A

101963871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 8099740-A-G

101963871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 8099740-A-T

101968707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8098645-A-G

101968851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8098514-T-C

101977878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8095723-C-G

http://identifiers.org/hco/11/GRCh38#101977933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8095676-A-C

101977933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8095676-A-T

101980523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8093233-C-T

101981135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8092705-C-G

101981135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8092705-C-T

101981503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8092574-C-T

101981620-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8092555-T-G

http://identifiers.org/hco/11/GRCh38#101981935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8092269-C-A

101981935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 8092269-C-T

101981941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 8092263-G-A

101981986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8092221-T-G

101986716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8087523-C-T

101986761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8087492-T-C

101986761-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8087492-T-G

101986924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 8087332-C-T

101987067-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8087201-A-T

101992564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8079758-A-G

http://identifiers.org/hco/11/GRCh38#101992621-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8079701-A-C

101992650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8079673-G-A

101992650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8079673-G-T

101992709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29264
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8079614-T-C