230906559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: 3 prime UTR variant
orthologous variants: 125398475-T-G

230906578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: 3 prime UTR variant
orthologous variants: 125398494-A-G

230906614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: 3 prime UTR variant
orthologous variants: 125398531-T-A

http://identifiers.org/hco/1/GRCh38#230906683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125398599-C-A

230906683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: 3 prime UTR variant
orthologous variants: 125398599-C-G

230906683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: 3 prime UTR variant
orthologous variants: 125398599-C-T

230906816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: 3 prime UTR variant
orthologous variants: 125398733-G-T

http://identifiers.org/hco/1/GRCh38#230906904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125398821-A-C

230906904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: 3 prime UTR variant
orthologous variants: 125398821-A-G

http://identifiers.org/hco/1/GRCh38#230906953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125398870-A-C

230906953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: synonymous variant
orthologous variants: 125398870-A-G

230907149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125399018-G-T

230907191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125399050-G-A

230907723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125399538-C-T

230909149-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125400594-T-A

230909171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125400616-T-C

230911376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125401012-G-A

230911376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125401012-G-T

230911391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125401034-A-T

230911456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125401087-A-G

230912439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125401596-C-T

http://identifiers.org/hco/1/GRCh38#230912608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125401946-C-A

230913728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125402488-T-C

230913729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125402489-A-G

230913729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125402489-A-T

230913775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125402533-G-A

230916174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125403058-C-G

230916201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125403088-T-C

230916222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125403109-A-G

230916222-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125403109-A-T

http://identifiers.org/hco/1/GRCh38#230920217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125405221-C-A

230920326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125405328-T-A

230920326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125405328-T-C

http://identifiers.org/hco/1/GRCh38#230920327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125405329-C-A

230920364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125405363-G-A

230920364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125405363-G-T

230920499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 125405730-G-T

http://identifiers.org/hco/1/GRCh38#230920504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125405735-A-C

230920528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125405759-G-C

http://identifiers.org/hco/1/GRCh38#230921013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125406381-C-A

230921014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125406382-C-T

http://identifiers.org/hco/1/GRCh38#230921374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125406680-C-A

230921374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125406680-C-T

http://identifiers.org/hco/1/GRCh38#230921389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125406695-C-A

230921519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125406825-T-A

230921519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125406825-T-C

230921585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125406874-T-A

230921585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125406874-T-C

230921636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125406917-T-G

230921648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125406927-T-C

http://identifiers.org/hco/1/GRCh38#230921652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125406931-C-A

230921652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125406931-C-T

230922031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125407423-G-A

230922075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125407466-C-T

230922212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125407570-G-A

230922281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125407630-A-T

230922431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125407746-A-G

230922431-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125407746-A-T

230922550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125407812-T-C

230922982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125408138-C-T

230923031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125408184-C-G

230923101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125408262-C-T

http://identifiers.org/hco/1/GRCh38#230923149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125408309-A-C

230923247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125408404-C-T

230923437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125408501-G-A

230923461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125408525-T-C

230923523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125408555-T-C

230923534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125408566-A-G

230923535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125408567-T-A

230923541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125408576-A-G

230923710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125408712-A-G

230923725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125408729-G-A

230923725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125408729-G-T

http://identifiers.org/hco/1/GRCh38#230923729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125408733-C-A

230923909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: synonymous variant
orthologous variants: 125408874-C-G

230923909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: synonymous variant
orthologous variants: 125408874-C-T

230923993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125408960-G-A

230923993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125408960-G-T

http://identifiers.org/hco/1/GRCh38#230924076-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125409034-A-C

http://identifiers.org/hco/1/GRCh38#230924079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125409037-A-C

230924079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125409037-A-G

230924080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125409038-G-A

230924080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125409038-G-T

230924732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125409802-G-C

230924732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125409802-G-T

230924855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: synonymous variant
orthologous variants: 125409936-T-C

230924855-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: synonymous variant
orthologous variants: 125409936-T-G

230924879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: synonymous variant
orthologous variants: 125409960-C-T

230924884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: missense variant
orthologous variants: 125409965-T-A

230924884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: missense variant
orthologous variants: 125409965-T-C

230924989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125410070-A-T

http://identifiers.org/hco/1/GRCh38#230924991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125410072-C-A

230924991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125410072-C-G

230924991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125410072-C-T

230925043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125410127-T-C

http://identifiers.org/hco/1/GRCh38#230925047-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125410131-A-C

230925047-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125410131-A-T

230925504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125410483-G-C

230925779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125410722-C-G

230925792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125410737-C-T

230928948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: synonymous variant
orthologous variants: 125411228-T-C

230929142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125411421-C-G

230929197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125411475-T-A

230929197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125411475-T-C

http://identifiers.org/hco/1/GRCh38#230929202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125411480-A-C

http://identifiers.org/hco/1/GRCh38#230929216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125411497-C-A

230930931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125414941-A-G

http://identifiers.org/hco/1/GRCh38#230930966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125414975-C-A

230930990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125414986-T-C

230931281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125415254-G-A

230931281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: intron variant
orthologous variants: 125415254-G-T

230931452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 125415424-T-A

230931452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 125415424-T-C

http://identifiers.org/hco/1/GRCh38#230931559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125415522-C-A

230931726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125415586-G-A

230931748-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 125415608-A-T

230931787-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 125415647-T-G

230931796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 125415656-C-G

230931799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 125415659-G-A

230931912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125415772-G-A

230931928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125415794-T-C

230931938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125415800-G-C

230931938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125415800-G-T

http://identifiers.org/hco/1/GRCh38#230931978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125415823-C-A

230931978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125415823-C-G

230931986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125415831-G-A

230931986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125415831-G-T

http://identifiers.org/hco/1/GRCh38#230932003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125415848-C-A

230932003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125415848-C-T

230932013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125415853-G-A

230932013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125415853-G-T

230932104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125415946-C-T

230932209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125416025-C-T

230932423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125416230-T-C

230932455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125416267-T-C

http://identifiers.org/hco/1/GRCh38#230932518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125416284-A-C

230932572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125416311-C-G

230932572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125416311-C-T

230933864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 125417101-A-G

230933886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125417123-T-C

230933972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125417197-T-A

230934261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125417397-T-C

230934859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, start_lost
orthologous variants: 125418437-C-T

230934866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125418444-G-A

230934990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125418515-C-G

230935033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125418557-C-T

230935217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125418665-T-C

230935439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125418868-C-T

230935551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125418928-G-C

230935768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125419047-A-G

230935768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125419047-A-T

230935853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125419122-T-C

230935957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125419191-A-G

230936014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125419220-G-T

230936034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125419236-G-A

230936034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125419236-G-T

230936062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125419253-G-A

230936351-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125419521-A-T

230936371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125419539-T-C

230936427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125419594-C-T

230936493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125419658-G-A

230936493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125419658-G-T

http://identifiers.org/hco/1/GRCh38#230936507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125419735-C-A

230936507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125419735-C-T

230936512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125419741-G-A

230936512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125419741-G-T

230936536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125419771-T-C

http://identifiers.org/hco/1/GRCh38#230936539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125419774-A-C

http://identifiers.org/hco/1/GRCh38#230936541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125419776-C-A

230936541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125419776-C-T

230936543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125419778-T-C

230936543-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125419778-T-G

230936626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125419849-G-T

http://identifiers.org/hco/1/GRCh38#230936697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125419910-C-A

230936697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125419910-C-G

230936922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125420078-T-C

230936981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125420136-G-A

230937283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125420354-T-C

230937308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125420373-T-C

230937345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125420402-T-C

230937873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125420789-A-T

230937889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125420808-T-C

230938144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125421096-C-G

230938271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125421225-T-C

230938408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125421349-T-C

230939340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125421525-G-A

230939340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125421525-G-C

230939340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125421525-G-T

230939604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125421765-C-T

230939979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125422041-A-G

230940333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125422293-T-G

230940384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125422333-A-G

230940617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125422551-T-C

http://identifiers.org/hco/1/GRCh38#230940638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125422572-C-A

230940638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125422572-C-G

230940638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125422572-C-T

http://identifiers.org/hco/1/GRCh38#230940643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125422577-C-A

230940648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125422582-T-G

http://identifiers.org/hco/1/GRCh38#230940649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125422583-C-A

230940649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125422583-C-G

http://identifiers.org/hco/1/GRCh38#230940677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125422612-C-A

230940677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125422612-C-T

230940684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125422619-T-C

230940697-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125422632-T-G

230941092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125422939-T-C

http://identifiers.org/hco/1/GRCh38#230941114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125422957-C-A

230941204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125423050-A-G

230941860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125423362-G-C

230942006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125423507-G-A

230942070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125423561-C-T

230942336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125423791-G-A

230942336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125423791-G-C

230943705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125424634-T-G

http://identifiers.org/hco/1/GRCh38#230943766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125424694-A-C

230943766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125424694-A-G

230943777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125424704-G-T

http://identifiers.org/hco/1/GRCh38#230943796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125424723-C-A

230943796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125424723-C-T

230943930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125424855-A-G

230943964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125424885-G-T

230943976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125424896-A-G

230943979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125424899-T-A

230943985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125424905-A-G

230944037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125424959-G-C

http://identifiers.org/hco/1/GRCh38#230944043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125424965-C-A

230944043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125424965-C-T

230944169-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125425069-T-G

230944212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125425114-T-C

230944212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125425114-T-G

230944347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125425245-T-C

230944449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125425341-A-G

230944623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125425486-A-G

230945064-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125426095-T-A

230945284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125426290-C-G

230945284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125426290-C-T

http://identifiers.org/hco/1/GRCh38#230945293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125426299-C-A

230945293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125426299-C-T

230945342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125426348-G-A

230945342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125426348-G-T

http://identifiers.org/hco/1/GRCh38#230945744-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125426705-A-C

230945807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125426772-G-A

230945894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125426829-A-T

230945959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125426883-T-A

230946006-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125426908-T-G

230946286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125427091-T-C

230946399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125427183-C-T

230946446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125427229-A-G

230946541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125427293-G-A

230946551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125427301-C-T

230947719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125428180-T-C

230947774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125428230-C-T

http://identifiers.org/hco/1/GRCh38#230947904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125428358-C-A

230947905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125428359-C-T

230948909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125428880-G-A

230948909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125428880-G-C

230948909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125428880-G-T

230949088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125429025-G-A

230950058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125430984-C-T

http://identifiers.org/hco/1/GRCh38#230951273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125433106-C-A

230951445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125433240-C-T

230951472-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125433282-T-G

230951912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125433835-A-G

230951943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125433865-C-G

230951943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125433865-C-T

230951960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125433882-C-G

230952002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125433900-C-T

http://identifiers.org/hco/1/GRCh38#230952457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125434319-C-A

230952676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125434516-G-A

230952791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125434653-A-G

230953217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125435262-T-A

230953550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125435776-T-G

230953983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125436342-G-A

230954045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125436398-C-T

230954243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125436557-A-G

230954244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125436558-T-C

230954250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125436564-A-G

230954255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125436569-A-G

230954255-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125436569-A-T

230954462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125436772-A-G

230954509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125436817-G-A

230954537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125436847-A-G

230954537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125436847-A-T

230957665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125438608-C-T

230957962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125438833-C-G

230957965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125438836-C-T

230958118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125439219-T-G

230958119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125439220-G-A

230958119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125439220-G-T

230958129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125439230-G-A

230958129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125439230-G-T

230958180-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125439281-T-A

230958198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125439331-G-A

230958252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 125439384-A-G

230958345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125439467-T-A

230958345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125439467-T-C

230958358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125439480-G-T

230958372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125439495-A-G

http://identifiers.org/hco/1/GRCh38#230958379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125439502-A-C

230958379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125439502-A-T

230958381-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125439504-A-T

http://identifiers.org/hco/1/GRCh38#230958427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125439547-C-A

230958427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125439547-C-T

230961195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125440914-G-A

230961254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 125440973-T-A

230961290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 125441009-C-G

230961322-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125441041-T-A

230961387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125441097-C-T

http://identifiers.org/hco/1/GRCh38#230961395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125441105-C-A

230961395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125441105-C-T

http://identifiers.org/hco/1/GRCh38#230961406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125441116-A-C

230975439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125446294-G-A

230975439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125446294-G-C

230975907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125447010-T-C

230976315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125447369-C-T

230976432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125447483-G-C

230977605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125447914-T-C

230978041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125448278-G-A

230978703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 125448607-G-A

230978703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26204
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 125448607-G-T