23506436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: 135923357-G-T

http://identifiers.org/hco/1/GRCh38#23506571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135923228-C-A

23506571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135923228-C-T

http://identifiers.org/hco/1/GRCh38#23506584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135923216-C-A

23506584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135923216-C-T

23506661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135923140-G-T

23506688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135923113-G-T

23506711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135923080-A-G

23506726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135923069-A-G

23506742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135923051-A-T

23506768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135923032-C-T

http://identifiers.org/hco/1/GRCh38#23506779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135923020-A-C

23506847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135922957-A-G

23506859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135922945-G-T

23506917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135922894-T-C

23506917-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135922894-T-G

http://identifiers.org/hco/1/GRCh38#23507164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135922728-C-A

23507619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135922572-G-A

23507619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135922572-G-T

http://identifiers.org/hco/1/GRCh38#23507677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135922516-C-A

23507680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135922513-G-A

23507680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135922513-G-T

23507915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135922321-A-G

http://identifiers.org/hco/1/GRCh38#23507980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135922257-C-A

http://identifiers.org/hco/1/GRCh38#23508003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135922216-C-A

23508003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135922216-C-T

23508021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135922190-G-T

23508030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135922181-T-G

http://identifiers.org/hco/1/GRCh38#23508051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135922162-C-A

http://identifiers.org/hco/1/GRCh38#23508053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135922160-C-A

23508054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135922159-T-G

23508056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135922157-G-A

23508131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135921910-G-A

23508131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135921910-G-T

23508137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135921904-A-G

23508139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135921902-C-T

23508188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135921852-G-A

23508188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135921852-G-T

23508189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135921851-C-T

23508209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135921833-T-C

23508299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135921761-A-G

23508348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135921712-T-C

23508424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135921626-C-T

23508449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135921596-T-C

23508519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135921517-G-T

http://identifiers.org/hco/1/GRCh38#23508613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135921425-C-A

http://identifiers.org/hco/1/GRCh38#23508616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135921422-C-A

23508625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135921411-T-C

23508625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135921411-T-G

23508635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135921401-T-C

23508682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135921345-G-A

23508881-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135921168-A-T

http://identifiers.org/hco/1/GRCh38#23508977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135921112-C-A

23508977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135921112-C-T

http://identifiers.org/hco/1/GRCh38#23508980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135921109-C-A

http://identifiers.org/hco/1/GRCh38#23508982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135921107-C-A

23508982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135921107-C-T

23509064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135921028-A-G

23509098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135920994-G-T

23509343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135920824-G-T

http://identifiers.org/hco/1/GRCh38#23509462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135920712-C-A

23509612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135920560-T-C

23509612-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135920560-T-G

23509621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135920551-T-C

23509621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135920551-T-G

23509672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135920533-A-T

http://identifiers.org/hco/1/GRCh38#23509685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135920519-C-A

23509685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135920519-C-G

23509691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135920512-T-C

http://identifiers.org/hco/1/GRCh38#23509697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135920506-C-A

23509697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135920506-C-T

23509733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135920470-C-T

23509753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135920445-G-T

23509761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135920437-G-C

23509761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135920437-G-T

23509788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135920419-G-C

23509883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 135920343-A-G

23510109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, missense_variant
orthologous variants: 135920093-G-A

23510109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, missense_variant
orthologous variants: 135920093-G-C

23510117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 135920085-G-T

http://identifiers.org/hco/1/GRCh38#23510119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135920083-C-A

23510127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, missense_variant
orthologous variants: 135920075-G-A

23510127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, missense_variant
orthologous variants: 135920075-G-C

23510129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 135920073-G-A

23510129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 135920073-G-T

23510171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: 135920037-T-C

http://identifiers.org/hco/1/GRCh38#23510205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135919988-C-A

23510205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: 135919988-C-T

23514225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: 135917414-G-A

23514351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: 135917273-A-G

http://identifiers.org/hco/1/GRCh38#23514474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135917159-A-C

23516180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: 135914423-A-G

23516205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: 135914398-G-T

http://identifiers.org/hco/1/GRCh38#23516303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135914319-C-A

23516303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: 135914319-C-G

23516303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: 135914319-C-T

23516339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: synonymous variant
orthologous variants: 135914296-G-A

23516339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: synonymous variant
orthologous variants: 135914296-G-T

23516348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: synonymous variant
orthologous variants: 135914287-G-A

23516348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: synonymous variant
orthologous variants: 135914287-G-T

http://identifiers.org/hco/1/GRCh38#23516379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135914256-C-A

23516379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135914256-C-G

23516379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135914256-C-T

23516462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135914173-C-T

23516490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135914145-G-A

23516490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135914145-G-T

23516566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135914079-G-A

23516576-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135914069-T-A

23516576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135914069-T-C

23516585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135914059-T-C

23516606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135914038-G-A

23516606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135914038-G-T

http://identifiers.org/hco/1/GRCh38#23516636-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135914013-A-C

23516811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135913867-G-C

23516811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135913867-G-T

http://identifiers.org/hco/1/GRCh38#23516812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135913866-C-A

23516812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135913866-C-G

23516985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135913700-T-G

23517093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135913600-A-G

23517128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135913565-T-C

23517271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135913474-A-T

23517279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135913466-G-A

23517279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135913466-G-T

23517634-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135913194-C-G

23518815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135911949-G-T

http://identifiers.org/hco/1/GRCh38#23519205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135911666-C-A

23519205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135911666-C-T

http://identifiers.org/hco/1/GRCh38#23519210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135911661-C-A

23519210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135911661-C-G

23519210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135911661-C-T

http://identifiers.org/hco/1/GRCh38#23519220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135911651-C-A

23519220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135911651-C-T

http://identifiers.org/hco/1/GRCh38#23519239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135911638-C-A

http://identifiers.org/hco/1/GRCh38#23519241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135911636-C-A

23519252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135911625-A-G

23519257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135911620-G-A

23520878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: 135908794-G-A

23520892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: 135908780-T-C

23520937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: missense variant
orthologous variants: 135908729-A-G

http://identifiers.org/hco/1/GRCh38#23521088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135908578-C-A

23521088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: 135908578-C-T

http://identifiers.org/hco/1/GRCh38#23521089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135908577-C-A

23521089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: 135908577-C-G

23521089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: 135908577-C-T

23521115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: 135908513-T-C

23521119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: 135908509-G-C

23521119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: 135908509-G-T

http://identifiers.org/hco/1/GRCh38#23521174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135908463-C-A

23521183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: 135908454-T-C

23521183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: 135908454-T-G

23521195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: 135908442-A-G

23521283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: 135908375-C-T

23521429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: 135908246-G-A

23521429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: 135908246-G-T

http://identifiers.org/hco/1/GRCh38#23521497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135908211-C-A

23521497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: 135908211-C-T

23521558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: 135908159-T-G

http://identifiers.org/hco/1/GRCh38#23521589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135908131-C-A

23521616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 135908098-A-G

23521687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 135908037-A-G

23521693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 135908030-C-T

23521696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 135908027-T-C

http://identifiers.org/hco/1/GRCh38#23521782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135907942-C-A

23521782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 135907942-C-T

23521821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 135907904-C-G

23521823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 135907900-G-A

23521823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 135907900-G-C

23521864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 135907859-T-C

23522023-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135907700-T-G

23522050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135907673-T-C

23522050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135907673-T-G

23522065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135907658-G-A

http://identifiers.org/hco/1/GRCh38#23522084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135907633-C-A

23522084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135907633-C-T

23522109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135907615-G-A

23522109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135907615-G-C

http://identifiers.org/hco/1/GRCh38#23522187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135907529-A-C

23522187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135907529-A-G

23522673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135907084-G-T

23523505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135906591-C-T

23523572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135906305-G-A

23523629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135906257-T-C

http://identifiers.org/hco/1/GRCh38#23523650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135906236-C-A

23524190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135906031-G-A

23524260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135905966-A-G

23524309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135905919-A-G

23524309-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135905919-A-T

http://identifiers.org/hco/1/GRCh38#23524364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135905868-C-A

23524364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135905868-C-T

http://identifiers.org/hco/1/GRCh38#23524368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135905865-A-C

23524368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135905865-A-G

23524369-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135905864-T-A

23524498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135905733-A-T

23524502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135905729-G-A

23524538-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135905693-T-A

http://identifiers.org/hco/1/GRCh38#23524560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135905664-C-A

23524560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135905664-C-T

23525030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135905375-C-T

http://identifiers.org/hco/1/GRCh38#23525306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135905074-A-C

23525921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135904639-G-C

23526151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135904444-T-C

23526179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135904416-C-T

23526254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135904332-T-C

http://identifiers.org/hco/1/GRCh38#23526296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135904288-C-A

23526372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135904216-G-A

23526821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135903836-G-A

http://identifiers.org/hco/1/GRCh38#23527177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135903517-C-A

http://identifiers.org/hco/1/GRCh38#23527191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135903510-C-A

23527192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135903509-C-G

23527257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135903467-G-A

http://identifiers.org/hco/1/GRCh38#23527365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135903367-C-A

23527365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135903367-C-T

23527509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135903254-G-A

23527604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135903192-C-T

23527618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135903178-T-C

23527780-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135903038-A-T

23527786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135903032-G-A

23528365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 135902298-C-T

23528526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: 135902122-C-T

23528850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, undefined
orthologous variants: 135901843-G-A

23528850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron_variant, undefined
orthologous variants: 135901843-G-C

23529171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: 135901726-A-G

23529961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: 135900864-G-A

23530097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: 135900743-G-T

http://identifiers.org/hco/1/GRCh38#23530243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135900610-C-A

23530467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: intron variant
orthologous variants: 135900427-G-T

23530838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 135900042-G-A

23530891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 135900009-C-T

23530978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 135899924-T-G

23531102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 135899828-C-T

23531103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 135899827-G-A

23531103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 135899827-G-C

http://identifiers.org/hco/1/GRCh38#23531139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3114
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#135899793-A-C