92833007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 108049100-A-G

http://identifiers.org/hco/1/GRCh38#92833073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#108049143-C-A

92833073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108049143-C-T

92833096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108049166-A-G

http://identifiers.org/hco/1/GRCh38#92833360-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#108049706-A-C

92833360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108049706-A-G

92833415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 108049762-G-C

92833515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108049855-A-G

92834195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108050251-T-C

92834303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108050399-G-A

92834303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108050399-G-T

92834533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108050549-G-A

92834584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108050590-A-G

92834762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108051120-T-G

92834811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 108051167-A-G

http://identifiers.org/hco/1/GRCh38#92836129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#108051477-A-C

92836129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108051477-A-G

92836460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108051793-G-A

92836460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108051793-G-C

92836486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108051803-A-G

92836580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108051859-G-A

92836580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108051859-G-T

92836581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108051860-A-G

92836581-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108051860-A-T

92836592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108051871-T-G

http://identifiers.org/hco/1/GRCh38#92836689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#108051917-C-A

http://identifiers.org/hco/1/GRCh38#92836842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#108052048-C-A

92836842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108052048-C-T

92836850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108052053-G-T

http://identifiers.org/hco/1/GRCh38#92836853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#108052056-A-C

92836882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108052085-G-T

http://identifiers.org/hco/1/GRCh38#92836910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#108052110-C-A

92837240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108052381-G-T

92837426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108052556-T-C

92837534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 108052661-G-C

92838056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108053085-A-G

92840431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108054955-T-C

92840431-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108054955-T-G

92840656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108055160-T-C

92840804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108055296-G-T

http://identifiers.org/hco/1/GRCh38#92840840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#108055331-C-A

92840840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108055331-C-G

92840840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108055331-C-T

http://identifiers.org/hco/1/GRCh38#92841908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#108055902-C-A

92841908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 108055902-C-G

92841908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 108055902-C-T

92841965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108055958-A-G

92841965-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108055958-A-T

92842061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108056142-T-C

92842088-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108056169-A-T

92842089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108056170-G-A

92842089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108056170-G-T

http://identifiers.org/hco/1/GRCh38#92842192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108056232-C-A

92842192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 108056232-C-G

92842689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 108056627-T-C

92842701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 108056639-G-A

92842791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 108056761-G-A

92842791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 108056761-G-T

http://identifiers.org/hco/1/GRCh38#92843001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108056951-C-A

92843050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 108056997-T-G

http://identifiers.org/hco/1/GRCh38#92843223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108057146-A-C

92843223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 108057146-A-G

http://identifiers.org/hco/1/GRCh38#92843234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108057157-C-A

92843234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 108057157-C-T

92843333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 108057232-G-A

92843333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 108057232-G-T

92843758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 108057645-A-G

92843842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 108057729-T-C

92843974-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, missense_variant
orthologous variants: 108057861-T-A

92843974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 108057861-T-C

92843974-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, missense_variant
orthologous variants: 108057861-T-G

92844031-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, missense_variant
orthologous variants: 108057918-T-A

92844037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 108057924-A-G

http://identifiers.org/hco/1/GRCh38#92844051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108057938-C-A

92844055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 108057942-G-A

92844121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 108058008-A-G

92844133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 108058020-A-G

92844189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 108058076-A-G

http://identifiers.org/hco/1/GRCh38#92847144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108059439-C-A

92847369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108059664-A-G

92850747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108061970-T-C

92850750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108061973-C-T

92850805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108062022-G-T

http://identifiers.org/hco/1/GRCh38#92850860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108062224-C-A

92850860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: synonymous variant
orthologous variants: 108062224-C-T

http://identifiers.org/hco/1/GRCh38#92850963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108062327-C-A

92850963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 108062327-C-T

92850971-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108062335-T-A

92851381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108062871-T-C

92851574-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108063019-A-T

92854210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108065023-T-C

92854684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108065430-C-G

92854720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108065465-T-G

92855292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108066050-T-C

http://identifiers.org/hco/1/GRCh38#92855310-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108066058-A-C

92858089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108068714-T-G

92858180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108068776-T-C

92858740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108069192-G-C

http://identifiers.org/hco/1/GRCh38#92858752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108069205-A-C

92858842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108069263-G-A

92859193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108069576-G-A

92864400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108070475-A-G

92864450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108070517-A-G

92867969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108071220-T-C

92868105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108071349-G-A

92875926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108072135-A-G

92876165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108072317-G-T

92876202-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108072353-T-G

92876485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108072635-A-G

92876486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108072636-T-A

92876486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108072636-T-C

92876535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108072683-T-C

http://identifiers.org/hco/1/GRCh38#92876572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108072720-C-A

92876572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108072720-C-G

92876572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108072720-C-T

92876596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108072744-G-A

92876596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108072744-G-T

92876739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108072843-T-C

92877228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108073621-C-T

http://identifiers.org/hco/1/GRCh38#92877249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108073642-C-A

92877249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108073642-C-T

92877497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108073889-C-T

92877587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108073988-G-T

92877599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108074000-T-C

92877684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108074270-G-A

92877684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108074270-G-C

92877853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108074455-A-G

92877855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108074457-G-T

92878028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108074582-A-G

92878162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108074707-G-A

92878162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108074707-G-T

92879997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108081204-C-G

92880082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108081288-T-C

http://identifiers.org/hco/1/GRCh38#92880273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108081416-A-C

92880308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108081451-T-A

92880453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108082400-A-G

92904067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108086031-T-C

92904280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108086195-G-C

92904339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108086255-G-A

92904468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108086379-A-G

92910268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108089558-A-G

92910270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108089560-C-G

92912259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108092922-G-A

92912259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108092922-G-C

92913103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108094533-G-C

92913332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108094785-G-T

92913398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108094839-G-A

92913431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108094871-T-C

92913864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108095244-T-C

92915658-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108095526-T-G

http://identifiers.org/hco/1/GRCh38#92915719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108095587-C-A

92915719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108095587-C-G

92916223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108096052-G-T

92916285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108096098-G-A

92916285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108096098-G-T

http://identifiers.org/hco/1/GRCh38#92916377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108096136-C-A

92916865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108096765-T-C

92917143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108096999-T-C

92917380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108097228-G-A

http://identifiers.org/hco/1/GRCh38#92919993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: -A-C

92920092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: -T-A

92920092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: -T-C

92920996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108098762-G-A

http://identifiers.org/hco/1/GRCh38#92921001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108098767-C-A

92921001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108098767-C-T

92921020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108098786-A-G

92921075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108098815-G-C

92921085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108098825-G-A

92921320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108099032-A-G

92921497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108099209-G-A

http://identifiers.org/hco/1/GRCh38#92922069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108099966-A-C

92922542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108100690-A-G

http://identifiers.org/hco/1/GRCh38#92922819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108100923-C-A

92922986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108101051-C-T

92923035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108101095-A-G

92923341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108101279-A-G

92923542-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108101428-T-G

http://identifiers.org/hco/1/GRCh38#92923968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108102239-A-C

92930086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: -G-C

92933547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108108983-A-G

92933551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108108987-A-G

92933642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108109086-G-A

92933664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108109105-T-C

92933721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108109164-G-C

92933743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108109186-G-A

92934967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108109764-T-C

92935582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108111749-G-A

92936192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108111966-A-G

92936202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108111976-T-C

92936337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108112105-G-A

92936752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108112174-A-G

92937488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108114157-C-T

92943466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108119997-T-A

92943654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108120375-T-G

92944978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108122995-C-T

92945469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108124457-A-G

92945477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108124470-G-A

92945523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108124517-A-T

http://identifiers.org/hco/1/GRCh38#92945740-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108124901-A-C

92945793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108124954-G-A

92945934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108125058-G-A

92956637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108128981-A-G

92957207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108129953-A-G

92957237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108129979-C-T

92957303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108130021-T-C

92957399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108130103-G-A

92957881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108130533-T-C

92958080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108130604-G-A

92958184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108130711-T-C

92958486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108132059-C-T

http://identifiers.org/hco/1/GRCh38#92958541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108132098-A-C

92958541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108132098-A-G

92960188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108133842-T-C

http://identifiers.org/hco/1/GRCh38#92960200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108133848-C-A

92960200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108133848-C-T

92960215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108133863-G-A

92960229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108133877-C-G

92960229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108133877-C-T

92960286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108133931-A-T

92960318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108133963-T-C

92960423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron_variant, undefined
orthologous variants: 108134075-G-A

92961017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108134625-C-T

92961061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108134671-C-T

92961281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108134741-G-A

92961281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108134741-G-C

92961281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108134741-G-T

http://identifiers.org/hco/1/GRCh38#92961302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108134760-C-A

92961302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108134760-C-G

92961302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: intron variant
orthologous variants: 108134760-C-T

92961415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: synonymous variant
orthologous variants: 108134854-G-A

92961415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: synonymous variant
orthologous variants: 108134854-G-C

92961415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: synonymous variant
orthologous variants: 108134854-G-T

92961508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: 5 prime UTR variant
orthologous variants: 108134930-G-A

92961508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: 5 prime UTR variant
orthologous variants: 108134930-G-C

92961508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: 5 prime UTR variant
orthologous variants: 108134930-G-T

92961511-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: 5 prime UTR variant
orthologous variants: 108134933-T-A

92961511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: 5 prime UTR variant
orthologous variants: 108134933-T-C

92961511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32213
most severe consequence: 5 prime UTR variant
orthologous variants: 108134933-T-G