21690823-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3 prime UTR variant
orthologous variants: 71218284-T-A

21690823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3 prime UTR variant
orthologous variants: 71218284-T-C

21690823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3 prime UTR variant
orthologous variants: 71218284-T-G

21690877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3 prime UTR variant
orthologous variants: 71218238-G-A

21690893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3 prime UTR variant
orthologous variants: 71218222-G-C

21691004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3 prime UTR variant
orthologous variants: 71218116-A-G

21691108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3 prime UTR variant
orthologous variants: 71218018-G-T

http://identifiers.org/hco/8/GRCh38#21691138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71217993-A-C

21691221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3 prime UTR variant
orthologous variants: 71217934-T-C

21691524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3 prime UTR variant
orthologous variants: 71217745-G-A

21691524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3 prime UTR variant
orthologous variants: 71217745-G-T

http://identifiers.org/hco/8/GRCh38#21691560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71217718-C-A

21691589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3 prime UTR variant
orthologous variants: 71217690-G-A

21691589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3 prime UTR variant
orthologous variants: 71217690-G-T

21691700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3 prime UTR variant
orthologous variants: 71217574-C-T

21692263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71217018-T-C

21692489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71216770-G-A

21692489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71216770-G-C

21692489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71216770-G-T

http://identifiers.org/hco/8/GRCh38#21692608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71216659-C-A

21692608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71216659-C-T

http://identifiers.org/hco/8/GRCh38#21692645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71216628-C-A

21692703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71216595-G-T

21692736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71216563-C-T

21692831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71216467-G-A

21692831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71216467-G-T

21692840-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71216458-T-A

21692840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71216458-T-C

http://identifiers.org/hco/8/GRCh38#21692853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71216444-C-A

21692853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71216444-C-T

http://identifiers.org/hco/8/GRCh38#21692873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71216424-C-A

21692873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71216424-C-T

21692894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71216415-T-A

21692894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71216415-T-C

http://identifiers.org/hco/8/GRCh38#21692910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71216399-C-A

21692910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71216399-C-G

21692910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71216399-C-T

21692928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71216383-G-C

21692928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71216383-G-T

21692944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71216367-G-T

21693032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71216300-C-G

21693032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71216300-C-T

http://identifiers.org/hco/8/GRCh38#21693049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71216284-C-A

http://identifiers.org/hco/8/GRCh38#21693068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71216266-C-A

21693068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71216266-C-T

21693187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71216068-G-A

21693187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71216068-G-T

21693197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71216058-G-C

21693197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71216058-G-T

21693280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 71215932-A-G

http://identifiers.org/hco/8/GRCh38#21693281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71215931-C-A

21693281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 71215931-C-T

21693293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 71215919-C-T

http://identifiers.org/hco/8/GRCh38#21693431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71215782-C-A

http://identifiers.org/hco/8/GRCh38#21693451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71215766-A-C

21693451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71215766-A-G

21693451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71215766-A-T

21693502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71215714-A-G

21693509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71215706-A-G

21693577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71215631-G-A

http://identifiers.org/hco/8/GRCh38#21693826-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71215243-A-C

21693826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71215243-A-G

21693826-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71215243-A-T

21693827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71215242-G-A

21693827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71215242-G-C

21693827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71215242-G-T

21693875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71215194-T-C

21693937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71215130-T-C

http://identifiers.org/hco/8/GRCh38#21693939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71215128-C-A

21694102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71215075-T-A

21694172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71215009-G-A

21694175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71215006-G-A

21694175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71215006-G-C

21694175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71215006-G-T

http://identifiers.org/hco/8/GRCh38#21694330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71214891-C-A

21694330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71214891-C-T

http://identifiers.org/hco/8/GRCh38#21694338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71214873-C-A

http://identifiers.org/hco/8/GRCh38#21694419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71214816-C-A

21694419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71214816-C-T

http://identifiers.org/hco/8/GRCh38#21694420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71214815-C-A

21694420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71214815-C-G

21694420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71214815-C-T

21694438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71214797-C-T

21694450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71214761-T-A

21694450-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71214761-T-G

21694575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71214644-T-C

http://identifiers.org/hco/8/GRCh38#21694578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71214641-C-A

21694578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71214641-C-T

http://identifiers.org/hco/8/GRCh38#21694625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71214608-C-A

http://identifiers.org/hco/8/GRCh38#21694626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71214607-A-C

21694626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71214607-A-G

21694628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71214605-A-G

21694952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71214304-T-C

21694988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71214271-T-C

21695147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71214129-T-C

21695147-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71214129-T-G

21695223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71214051-A-G

21695223-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71214051-A-T

21695285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71213987-C-G

21695572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71213699-C-T

21695594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71213677-G-A

21695657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71213614-G-A

http://identifiers.org/hco/8/GRCh38#21695918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71213398-C-A

21698146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71209941-T-C

21698158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71209929-C-T

21698205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71209882-A-G

21698517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71209608-G-T

21698579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71209539-C-T

http://identifiers.org/hco/8/GRCh38#21699090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71208910-C-A

21699135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71208851-G-A

21699136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71208850-G-A

http://identifiers.org/hco/8/GRCh38#21700422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71208351-C-A

21700422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71208351-C-T

http://identifiers.org/hco/8/GRCh38#21700474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71208311-C-A

21700573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71208196-G-A

21700606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71208163-G-C

21700819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71207952-C-T

21702594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71206097-T-C

http://identifiers.org/hco/8/GRCh38#21702709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71205984-A-C

21702709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71205984-A-G

http://identifiers.org/hco/8/GRCh38#21702723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71205966-C-A

21702723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71205966-C-T

21703030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71205631-T-C

21704369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71205239-C-T

21704678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71204928-C-T

21704790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71204813-G-C

http://identifiers.org/hco/8/GRCh38#21704851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71204749-C-A

21704851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71204749-C-G

21704851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71204749-C-T

21704866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71204731-G-A

21704866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71204731-G-T

21704936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71204646-G-A

http://identifiers.org/hco/8/GRCh38#21705250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71204375-A-C

21705288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71204331-T-C

http://identifiers.org/hco/8/GRCh38#21705556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71204055-A-C

21705556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71204055-A-G

21705719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71203941-C-T

21705814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71203882-G-A

21705814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71203882-G-T

http://identifiers.org/hco/8/GRCh38#21705826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71203876-C-A

21705852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71203849-T-C

21705852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71203849-T-G

21705858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71203843-G-A

21705858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71203843-G-T

21705887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71203804-G-C

21705887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71203804-G-T

http://identifiers.org/hco/8/GRCh38#21706277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71203377-C-A

21706277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71203377-C-T

21706387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71203252-C-G

21706390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71203249-G-A

21706398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71203241-G-A

http://identifiers.org/hco/8/GRCh38#21706493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71203151-C-A

21706517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71203141-C-G

21706522-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71203136-T-A

21706527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71203131-G-A

21706542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71203116-G-A

21706611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71203045-T-C

http://identifiers.org/hco/8/GRCh38#21706987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71202723-C-A

21706987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71202723-C-T

21708944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71202505-C-T

21709201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71202298-C-T

http://identifiers.org/hco/8/GRCh38#21709254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71202231-C-A

21709441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71202055-C-T

21709747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71201743-G-A

21709806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71201682-G-A

21709814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71201674-C-T

21709835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71201653-C-T

21709980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71201523-G-A

21709981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71201522-C-T

21710033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71201471-G-A

21710089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71201412-T-C

21710089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71201412-T-G

http://identifiers.org/hco/8/GRCh38#21710121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71201386-C-A

21710121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71201386-C-T

21710332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71201209-C-G

http://identifiers.org/hco/8/GRCh38#21710502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71201087-C-A

21710536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71201044-C-T

http://identifiers.org/hco/8/GRCh38#21710599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71200981-A-C

21710696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71200877-C-T

21710804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71200785-C-G

21711015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71200581-T-A

21711228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71200381-C-T

21711286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71200322-G-A

21711492-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71200146-T-A

21711498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71200140-G-A

21711498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71200140-G-C

21711498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71200140-G-T

21711633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71200023-T-C

21711643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71200013-A-G

21713527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71199690-C-T

21713703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71199565-A-T

21713790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71199499-C-T

21713847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71199443-T-A

21713998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71199298-G-A

21714040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71199260-T-C

http://identifiers.org/hco/8/GRCh38#21714825-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71198303-A-C

http://identifiers.org/hco/8/GRCh38#21714837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71198291-C-A

21714949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71198178-G-A

21717593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71192695-A-G

21718854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71192184-T-C

21718857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71192181-G-A

http://identifiers.org/hco/8/GRCh38#21718909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71192138-A-C

21719013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71192040-C-T

21719030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71192030-A-G

21719030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71192030-A-T

21719038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71192022-T-C

21719071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71191996-G-A

http://identifiers.org/hco/8/GRCh38#21719171-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71191891-A-C

http://identifiers.org/hco/8/GRCh38#21719172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71191890-C-A

21719172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71191890-C-G

21719215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71191847-T-C

21719390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71191695-T-G

http://identifiers.org/hco/8/GRCh38#21719408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71191679-C-A

21719435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71191652-T-C

21719734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71191351-T-C

21719740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71191345-G-A

21719743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71191342-G-A

21719850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71191237-G-A

21719910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71191176-G-T

21720042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71191046-C-T

21720043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71191045-C-T

21720171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71190911-G-A

21720171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71190911-G-T

21720320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71190789-G-C

21720472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71190640-G-T

http://identifiers.org/hco/8/GRCh38#21720498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71190611-C-A

21720985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71190033-G-A

21721015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71190006-A-G

http://identifiers.org/hco/8/GRCh38#21721245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71189766-A-C

21721484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71189527-C-T

21721485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71189526-G-A

21721537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71189455-C-T

http://identifiers.org/hco/8/GRCh38#21721707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71189276-C-A

21721781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71189188-G-C

21721931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71189050-T-C

21723468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71187931-T-C

21723526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71187873-C-T

21723678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71187734-G-A

21723717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71187697-G-A

21723730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71187685-A-G

http://identifiers.org/hco/8/GRCh38#21723741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71187674-C-A

21723741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71187674-C-T

21723788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71187625-T-C

21723817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71187597-A-G

21724440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71187043-C-T

21724452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71187032-T-G

21724464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71187020-G-A

21724489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71186999-A-G

http://identifiers.org/hco/8/GRCh38#21724526-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71186959-A-C

21724640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71186845-G-C

21724698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71186813-G-A

21724700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71186811-G-A

21724714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71186796-C-T

http://identifiers.org/hco/8/GRCh38#21724811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71186718-C-A

21724910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71186591-T-C

http://identifiers.org/hco/8/GRCh38#21725307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71186014-C-A

21725827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71185413-G-A

21725862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71185381-G-A

21725895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71185346-C-T

21725914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71185327-G-A

21726045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71185192-C-T

http://identifiers.org/hco/8/GRCh38#21726180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71185095-C-A

21726180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71185095-C-T

http://identifiers.org/hco/8/GRCh38#21726182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71185093-C-A

21726188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71185087-A-G

21726320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71184979-G-A

21727102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71184770-T-C

21727102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71184770-T-G

21727472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71184536-C-T

21727483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71184527-G-A

21727708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71184321-T-C

21727764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71184273-T-C

21727962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71184066-T-C

21728007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71184032-G-A

21728212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71183848-G-C

21729516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71183275-G-A

21730641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71181958-C-T

21730978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71180322-G-A

21731041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71180262-C-T

21731117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71180196-T-C

21731470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71179872-T-C

21731505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71179828-C-T

http://identifiers.org/hco/8/GRCh38#21731508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71179825-C-A

21731639-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71179696-T-A

21731644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71179691-G-A

21731717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71179618-C-T

21731754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71179582-C-T

21731999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71179321-G-A

21732261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71179049-G-C

21732761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71178523-C-G

21732820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71178462-C-G

http://identifiers.org/hco/8/GRCh38#21732901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71178296-C-A

21732901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71178296-C-G

21732901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71178296-C-T

21733257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71177992-C-T

http://identifiers.org/hco/8/GRCh38#21733323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71177940-C-A

21733323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71177940-C-G

21733323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71177940-C-T

21733335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71177931-C-T

21733651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71177598-T-C

http://identifiers.org/hco/8/GRCh38#21733681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71177568-C-A

21733897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71177352-C-G

21733897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71177352-C-T

21734019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71177231-T-G

21734069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71177183-C-G

21734070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71177182-C-T

21734297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71176971-C-T

21736272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71174656-T-C

http://identifiers.org/hco/8/GRCh38#21736407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71174522-C-A

21736829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71174183-T-A

21736838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71174174-A-G

21737059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71173974-C-G

21737104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71173941-G-A

21737658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71173831-C-G

21737924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71173584-C-T

21737956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71173553-T-C

http://identifiers.org/hco/8/GRCh38#21738288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71173311-C-A

21738665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71172945-C-T

21739154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71172531-G-C

21739257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71172437-G-A

21742060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71170667-A-T

21742109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71170614-T-C

21742207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71170556-G-A

21742505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71170242-G-A

21742531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71170218-C-T

21742631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71170122-G-A

21742668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71170086-C-T

http://identifiers.org/hco/8/GRCh38#21742672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71170078-C-A

21742672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71170078-C-T

21742786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71169957-A-G

21742830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71169913-C-T

21742987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71169744-G-A

21742987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71169744-G-C

21743084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71169651-T-C

21743143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71169600-C-T

http://identifiers.org/hco/8/GRCh38#21743335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71169464-C-A

21743335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71169464-C-G

21743335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71169464-C-T

21743336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71169463-G-A

http://identifiers.org/hco/8/GRCh38#21743422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71169386-A-C

21743560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71169274-C-T

http://identifiers.org/hco/8/GRCh38#21743578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71169256-C-A

21743589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71169245-G-A

21743611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71169224-T-C

21743674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71169162-G-A

21743677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71169159-A-G

21744116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71168730-C-T

21744292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71168633-A-G

21744292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71168633-A-T

21744897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71167904-T-C

21745131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71167632-G-A

21745289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71167507-C-T

21745348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71167466-A-G

21745364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71167450-G-A

21745375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71167439-G-C

21745403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71167393-G-A

21745506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71167300-G-A

21745723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71167073-T-C

21745805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71167007-G-T

21745854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71166959-G-A

21745998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71166912-G-A

21746052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71166870-A-G

http://identifiers.org/hco/8/GRCh38#21746224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71166728-A-C

http://identifiers.org/hco/8/GRCh38#21746275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71166685-C-A

21746434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71166502-G-A

21746441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71166495-T-C

21746453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71166483-C-T

21746592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71166348-C-T

21746962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71166060-G-A

21747069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71165914-T-C

21747075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71165908-G-A

21747245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71165725-T-C

21747245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71165725-T-G

21747552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71165412-C-G

21747552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71165412-C-T

http://identifiers.org/hco/8/GRCh38#21747651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71165293-C-A

21747651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71165293-C-T

21747697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71165248-A-G

21747702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71165243-A-G

21747893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71165104-A-G

21747959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71165039-C-T

21748039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71164951-T-C

21748262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71164739-A-G

http://identifiers.org/hco/8/GRCh38#21748363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71164637-C-A

21748363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71164637-C-T

21748579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71164468-G-T

21748607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71164439-T-C

21748628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71164417-A-G

21748793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71164265-C-T

http://identifiers.org/hco/8/GRCh38#21748959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71164150-A-C

21750296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71163794-G-C

21750366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71163708-G-A

21750366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71163708-G-C

21750366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71163708-G-T

21750410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71163658-G-A

http://identifiers.org/hco/8/GRCh38#21750473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71163606-C-A

21750500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71163575-G-T

21750535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71163557-T-A

21750535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71163557-T-C

21750546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71163546-G-A

21750546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71163546-G-T

21750548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71163544-G-A

21750548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71163544-G-T

http://identifiers.org/hco/8/GRCh38#21750553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71163539-C-A

21750553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71163539-C-G

21750756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 71163342-T-C

21750953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71163145-A-G

21751048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71163065-G-A

21751048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71163065-G-T

http://identifiers.org/hco/8/GRCh38#21751078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71163027-C-A

21751078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71163027-C-G

21751078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71163027-C-T

http://identifiers.org/hco/8/GRCh38#21751092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71163013-C-A

21751183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71162915-T-C

http://identifiers.org/hco/8/GRCh38#21751335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71162731-C-A

http://identifiers.org/hco/8/GRCh38#21751411-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71162230-A-C

21751556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71162077-C-T

21751587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71162039-T-G

21751696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71161930-G-A

21751696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71161930-G-C

21751742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71161887-G-T

http://identifiers.org/hco/8/GRCh38#21751824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71161819-C-A

21751938-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71161709-A-T

21751982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71161667-C-T

21752144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71161492-C-G

21752159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71161477-T-C

21752227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71161412-C-T

21752312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71161339-G-C

21752340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71161306-A-G

http://identifiers.org/hco/8/GRCh38#21752482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71161193-C-A

21752482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71161193-C-G

21752559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71161119-T-C

21752667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71161031-A-G

21752726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71160987-G-A

21753709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71160519-G-T

21753717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71160511-A-T

21753752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71160480-C-T

21753772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71160451-C-T

21753972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71160203-G-A

21753972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71160203-G-T

21754092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71160096-T-A

21754116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71160074-C-G

21754116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71160074-C-T

21754381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71159842-T-C

21754392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71159831-G-A

http://identifiers.org/hco/8/GRCh38#21754488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71159802-C-A

21754611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71159775-A-T

21754843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71159688-G-A

21755125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71159432-T-C

21755125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71159432-T-G

21755274-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71159289-T-A

21755312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71159261-A-G

21755321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71159252-G-A

21755373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71159206-A-G

21755634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71158379-T-C

21755634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71158379-T-G

21755940-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71158076-T-G

21755964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71158059-G-A

21756068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71157952-G-A

21756506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71157534-G-A

21756506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71157534-G-C

21757306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71156788-C-T

http://identifiers.org/hco/8/GRCh38#21757661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71156552-A-C

21758270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71155964-G-A

21758270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71155964-G-T

21758398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71155844-G-A

21758400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71155842-G-C

21758410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71155834-A-G

21759916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71155514-G-A

21760045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71155403-C-T

21760182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71155240-G-A

21760182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71155240-G-C

21760252-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71155180-T-A

21760252-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71155180-T-G

21760336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71155070-A-G

21760532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71154908-A-G

21760554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71154886-G-C

21760675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71154784-G-A

21761549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71154019-C-T

21761567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71154000-C-T

21762123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71153368-C-T

21762156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71153333-C-T

21762186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71153292-T-C

21762487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71153035-C-G

21763770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71152688-C-G

21763770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71152688-C-T

21763946-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71152543-A-T

21765694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71150823-G-A

21765807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71150712-T-C

21765907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71150630-C-T

21766516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71149955-T-G

http://identifiers.org/hco/8/GRCh38#21766520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71149951-C-A

21766665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71149767-A-G

21766808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71149596-G-A

21766808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71149596-G-T

21766832-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71149573-T-A

21766832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71149573-T-C

http://identifiers.org/hco/8/GRCh38#21766946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71149463-C-A

21766946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71149463-C-G

21767098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71149294-C-T

21767192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71149181-C-T

21767205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71149168-C-G

http://identifiers.org/hco/8/GRCh38#21767361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71148981-C-A

21767361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71148981-C-T

21767818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71148505-T-C

http://identifiers.org/hco/8/GRCh38#21767909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71148414-C-A

21767918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71148405-C-T

21767958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71148364-C-G

21768028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71148307-C-T

21768088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71148245-C-T

21768095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71148238-C-T

21768400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71147982-T-C

21768415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71147970-C-T

21768511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71147895-T-G

http://identifiers.org/hco/8/GRCh38#21768679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71147768-C-A

21768687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71147760-G-T

21768793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71147654-C-T

21768801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71147646-C-G

21768879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71147615-C-T

21768980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71146917-G-A

21769002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71146895-T-C

21769295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71146632-A-G

21769295-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71146632-A-T

21769316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71146614-T-A

21769316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71146614-T-C

21769316-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71146614-T-G

21769327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71146603-C-T

21769406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71146493-A-G

21769644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71146251-T-G

21769715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71146181-C-T

21769793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71146110-G-A

21769793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71146110-G-C

21769892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71146033-G-A

21770009-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71145937-T-A

21770038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71145907-C-T

http://identifiers.org/hco/8/GRCh38#21770282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71145673-A-C

21770283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71145672-A-G

21770357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71145604-G-C

21770357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71145604-G-T

21770396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71145571-A-T

21770444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71145543-T-A

21770492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71145494-C-T

http://identifiers.org/hco/8/GRCh38#21770508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71145478-C-A

http://identifiers.org/hco/8/GRCh38#21770757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71145256-C-A

21770757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71145256-C-G

21771084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -C-T

21771173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -A-G

21771234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71144442-T-C

21771261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71144416-C-G

21771324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71144355-A-G

21771415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71144266-C-T

21771428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71144250-G-A

21771473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71144207-T-C

21771858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71143830-C-T

21772215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71143512-G-A

21772652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71142805-G-A

21773009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71142477-G-A

http://identifiers.org/hco/8/GRCh38#21773024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71142462-C-A

21773099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71142387-G-A

21773099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71142387-G-C

21773141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71142347-G-A

21773166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71142324-A-T

http://identifiers.org/hco/8/GRCh38#21773358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71142129-A-C

21773364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71142124-C-G

21773649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71141338-T-C

21773816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71141211-G-A

21774017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71141024-A-G

21774067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71140988-T-C

21774549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71139416-C-T

21774550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71139415-T-A

21774652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71139329-G-T

21774701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71139269-G-A

21774787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71139197-C-T

21774804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71139176-C-T

http://identifiers.org/hco/8/GRCh38#21774810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71139170-C-A

21774949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71139032-A-G

21774949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71139032-A-T

21774952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71139029-C-T

21775031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 71138951-G-A

21775031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 71138951-G-C

21775031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 71138951-G-T

http://identifiers.org/hco/8/GRCh38#21775082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71138901-C-A

21775082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71138901-C-G

21775082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71138901-C-T

http://identifiers.org/hco/8/GRCh38#21775374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71138671-C-A

21775457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71138584-G-A

21775655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71138437-G-A

21775814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71138284-G-A

http://identifiers.org/hco/8/GRCh38#21775828-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71138270-A-C

21775940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71138158-T-C

http://identifiers.org/hco/8/GRCh38#21776247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71137878-C-A

21776247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71137878-C-G

21777150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71137349-T-G

http://identifiers.org/hco/8/GRCh38#21777210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71137297-A-C

21778031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71136620-C-T

21778185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71136460-G-A

21778426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71136278-G-A

21778437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71136267-A-G

21779532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71135663-G-T

21779585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71135610-G-A

21779668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71135529-T-A

21779729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71135469-G-A

21779729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71135469-G-T

http://identifiers.org/hco/8/GRCh38#21779757-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71135441-A-C

21779757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71135441-A-G

21779774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71135415-A-G

21779864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71135331-C-T

21781613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71134261-C-T

21781751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71134130-A-G

21781845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71134039-G-C

21782308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71133681-T-A

21782308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71133681-T-C

21782522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71133578-G-A

21782522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71133578-G-C

21782522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71133578-G-T

21782670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71133439-C-T

21782698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71133411-G-A

http://identifiers.org/hco/8/GRCh38#21782743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71133366-C-A

http://identifiers.org/hco/8/GRCh38#21783045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71133083-C-A

21783045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 71133083-C-T

21783084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 71133050-G-A

21783133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 71133016-G-A

21783133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 71133016-G-T

21783172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71132977-G-A

21783172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71132977-G-T

http://identifiers.org/hco/8/GRCh38#21783190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71132959-C-A

21783190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71132959-C-T

21783191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71132958-A-G

21783201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71132945-G-A

21783201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71132945-G-T

http://identifiers.org/hco/8/GRCh38#21783230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71132917-C-A

21783230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71132917-C-G

21783377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71132834-G-A

21783572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71132664-G-A

21783606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71132634-A-G

21783696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71132547-G-A

21783714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71132529-C-T

21783715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71132528-G-A

21784030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71132223-C-T

http://identifiers.org/hco/8/GRCh38#21784092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71132185-A-C

21784187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71132106-G-A

21784187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71132106-G-C

21784327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71131968-G-T

21784435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71131859-G-T

http://identifiers.org/hco/8/GRCh38#21784450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#71131838-A-C

21784450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71131838-A-G

21784552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71131735-G-A

21784610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71131694-C-G

21784610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71131694-C-T

21785025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71131276-C-T

21785141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71131158-C-T

21785578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71130787-G-A

21785578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71130787-G-T

21785856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71130530-C-T

21785958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71130422-G-A

21785985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71130396-T-C

21785990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71130391-T-G

21786072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71130310-G-A

21786091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71130291-A-G

21787237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71129194-G-A

21787281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71129167-G-A

21787281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71129167-G-C

21787281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71129167-G-T

21787738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71128752-C-T

21788130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71128322-G-A

21788284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71128160-G-T

21788334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71128108-G-A

21788334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71128108-G-T

21788345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71128097-G-A

21788345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71128097-G-T

21788359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71128083-G-A

21788359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71128083-G-T

21788453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71127989-G-A

21788453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71127989-G-T

http://identifiers.org/hco/8/GRCh38#21788486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#71127952-C-A

21788486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 71127952-C-T

21788715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71127734-C-G

http://identifiers.org/hco/8/GRCh38#21788797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71127641-C-A

21788797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71127641-C-T

21788820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 71127603-T-A

21788820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 71127603-T-C

21788822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 71127601-T-C

21788822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 71127601-T-G

21788833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 71127590-C-T

21788964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71127444-G-A

21788964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71127444-G-C

21788964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71127444-G-T

21789022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron_variant, undefined
orthologous variants: 71127387-C-T

21789068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71127348-G-A

21789068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71127348-G-T

21789069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71127347-A-G

21789078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron_variant, undefined
orthologous variants: 71127338-A-G

21789117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71127299-G-A

21789117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71127299-G-C

21789117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71127299-G-T

21789203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 71127217-G-A

21789203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 71127217-G-T

21789205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71127215-A-G

http://identifiers.org/hco/8/GRCh38#21789310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71127112-C-A

21789312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71127110-C-T

http://identifiers.org/hco/8/GRCh38#21789343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71127079-C-A

21789343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71127079-C-G

http://identifiers.org/hco/8/GRCh38#21789371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71127050-C-A

21789383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71127038-G-T

21789391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71127030-G-A

21789391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71127030-G-T

21789411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71127018-G-C

21789424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71127005-C-T

21789429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71127000-G-A

21789545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71126884-C-G

21789562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71126872-C-T

21789604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71126830-C-T

21789692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71126770-C-G

21789770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71126661-C-T

21789907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71126531-G-C

21790063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71126333-G-A

21790212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron_variant, undefined
orthologous variants: 71126180-G-A

21790227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71126162-C-T

21790231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron_variant, undefined
orthologous variants: 71126157-G-A

http://identifiers.org/hco/8/GRCh38#21790232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#71126156-C-A

21790232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron_variant, undefined
orthologous variants: 71126156-C-T

21790275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron_variant, undefined
orthologous variants: 71126119-T-C

21790290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71126079-G-A

http://identifiers.org/hco/8/GRCh38#21790615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71125776-A-C

21790709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71125705-G-A

21790762-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71125665-A-T

http://identifiers.org/hco/8/GRCh38#21790768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71125659-C-A

21790894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71125560-G-T

21790938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71125516-G-C

21790994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71125455-G-A

http://identifiers.org/hco/8/GRCh38#21791122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71125378-A-C

21791245-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71125269-A-T

21791364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71125145-G-C

http://identifiers.org/hco/8/GRCh38#21791475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71125062-A-C

21791982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71124619-C-T

21792674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71123837-T-C

21793166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71123671-T-G

21793239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71123598-C-T

21793303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71123542-C-T

21793368-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71123482-T-G

21793394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71123459-G-C

21793516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71123285-A-G

21793764-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71123097-T-G

21793774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71123087-C-T

21793867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71123002-T-G

21794791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71122806-C-G

21795078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71122525-G-A

21795923-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71122070-A-T

21796059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71121951-A-T

21796214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71121808-T-C

21796383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71121677-G-A

21796556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71121473-A-G

21796557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71121472-G-A

21796561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71121468-T-C

21796758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71121269-T-C

21796849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71121166-G-A

21797817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71121148-C-T

21797870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71121099-T-C

21797870-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71121099-T-G

21797889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71121080-G-A

21797889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71121080-G-T

21797906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71121073-T-C

21798070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71120938-A-G

21798100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71120898-C-G

21798154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71120821-G-A

21798154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71120821-G-T

21798477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71119851-C-T

21799186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71119162-T-C

21799194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71119154-G-A

21799673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71118952-C-T

21800019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71118588-G-A

21800368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71118235-C-T

21800375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71118228-G-A

http://identifiers.org/hco/8/GRCh38#21800391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71118212-C-A

21800410-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71118193-T-A

21800606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71117985-G-A

21801192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71117784-A-G

21801216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71117756-G-A

21801520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71117477-C-G

21802688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71117271-A-G

21802747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71117212-A-G

21802747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71117212-A-T

21802753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71117206-G-A

21803052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71116508-A-G

http://identifiers.org/hco/8/GRCh38#21803493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71116090-C-A

21803506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71116077-A-G

21804146-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71115663-A-T

http://identifiers.org/hco/8/GRCh38#21804267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71115602-C-A

21804267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71115602-C-G

21804704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71115249-G-A

21804725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71115228-G-T

21804862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71115085-C-G

21804895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71115051-A-G

http://identifiers.org/hco/8/GRCh38#21804902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71115045-C-A

21804902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71115045-C-T

21804937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71115011-G-C

21804937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71115011-G-T

http://identifiers.org/hco/8/GRCh38#21804992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71114958-C-A

http://identifiers.org/hco/8/GRCh38#21805006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71114944-C-A

http://identifiers.org/hco/8/GRCh38#21805272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71114675-C-A

21805889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71111940-A-G

21806981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71111538-G-T

21808171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71110723-G-A

21808171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71110723-G-T

21808489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71110425-A-G

21808490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71110424-G-A

21808502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71110412-T-C

21809118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71109804-T-C

21809137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71109785-A-G

21809258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71109686-G-A

http://identifiers.org/hco/8/GRCh38#21809759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71109502-C-A

21809759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71109502-C-T

21809818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71109446-C-G

21809922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71109379-G-T

21810027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71109275-C-T

21810161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71109191-C-T

21810746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71108588-G-A

21810966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71108012-A-G

21811128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71107851-C-T

21811225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71107737-C-G

21811306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71107660-T-C

21811379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71107591-A-G

21811632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: 71103945-G-A

http://identifiers.org/hco/8/GRCh38#21812094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71103279-C-A

http://identifiers.org/hco/8/GRCh38#21812246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#71103151-C-A

21812246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4244
most severe consequence: 5 prime UTR variant
orthologous variants: 71103151-C-T