1508044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 80178789-G-A

1508044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 80178789-G-C

http://identifiers.org/hco/19/GRCh38#1508126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#80178876-A-C

1508126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80178876-A-G

1508127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80178877-G-A

1508127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80178877-G-T

1508133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80178883-G-A

1508133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80178883-G-T

1508134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80178884-C-T

1508177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80178945-G-A

1508177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80178945-G-C

1508177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80178945-G-T

http://identifiers.org/hco/19/GRCh38#1508184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80178952-A-C

http://identifiers.org/hco/19/GRCh38#1508194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80178972-C-A

1508194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80178972-C-G

1508194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80178972-C-T

http://identifiers.org/hco/19/GRCh38#1508240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80179059-C-A

1508240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80179059-C-T

1508262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80179114-T-C

1508262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80179114-T-G

1508382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80179351-G-A

1508393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80179368-G-A

1508393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80179368-G-T

http://identifiers.org/hco/19/GRCh38#1508395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80179382-C-A

http://identifiers.org/hco/19/GRCh38#1508411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#80179403-C-A

1508411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80179403-C-G

1508411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80179403-C-T

http://identifiers.org/hco/19/GRCh38#1508467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80179457-C-A

1508467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80179457-C-T

http://identifiers.org/hco/19/GRCh38#1509698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80180283-A-C

1509954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80180528-C-T

http://identifiers.org/hco/19/GRCh38#1510127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80180644-C-A

1510407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 80180916-G-T

http://identifiers.org/hco/19/GRCh38#1510566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80181098-C-A

1510566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80181098-C-T

http://identifiers.org/hco/19/GRCh38#1510574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80181106-C-A

1510574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80181106-C-T

1510593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80181119-G-A

1510668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80181185-G-A

1510668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80181185-G-T

1510862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80181364-A-G

1510862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80181364-A-T

1510946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80181434-A-G

1511060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80181556-A-G

1511091-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80181594-T-G

1511700-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80183191-T-A

1511801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80183296-C-T

1511860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80183379-G-A

1511860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80183379-G-T

http://identifiers.org/hco/19/GRCh38#1512130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80183628-C-A

1512130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80183628-C-T

http://identifiers.org/hco/19/GRCh38#1512857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#80184140-C-A

1512857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80184140-C-T

1512912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80184153-T-A

1512912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80184153-T-C

http://identifiers.org/hco/19/GRCh38#1512971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80184198-C-A

1512971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80184198-C-T

1513116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 80184340-G-A

http://identifiers.org/hco/19/GRCh38#1513475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80184807-C-A

1513475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80184807-C-T

http://identifiers.org/hco/19/GRCh38#1513494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80184826-C-A

1513494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80184826-C-G

1513494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80184826-C-T

1513548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80184872-G-A

1513548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80184872-G-T

1513567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 80184889-G-A

1514017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, undefined
orthologous variants: 80185220-C-T

1514166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, undefined
orthologous variants: 80185322-G-A

1514675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron variant
orthologous variants: 80185731-A-G

1514928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron variant
orthologous variants: 80185965-A-G

1515027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron variant
orthologous variants: 80186067-A-G

1517991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80187583-T-C

1518011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80187603-T-G

1518258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80187823-T-C

1518316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80187889-T-C

1518326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80187899-T-C

1518332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80187905-G-A

http://identifiers.org/hco/19/GRCh38#1520451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80189060-C-A

1520616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80189224-C-G

1520616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80189224-C-T

1521785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80190228-G-A

1521786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80190229-C-T

1522095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80190499-G-A

1522902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron variant
orthologous variants: 80191338-C-T

1522950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron variant
orthologous variants: 80191390-T-C

1523079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron variant
orthologous variants: 80191521-G-A

1523079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron variant
orthologous variants: 80191521-G-C

1523220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron variant
orthologous variants: 80191650-A-T

http://identifiers.org/hco/19/GRCh38#1523225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80191655-A-C

http://identifiers.org/hco/19/GRCh38#1523964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80192226-C-A

1523964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron variant
orthologous variants: 80192226-C-G

1523964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron variant
orthologous variants: 80192226-C-T

1523973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron variant
orthologous variants: 80192235-G-A

1523973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron variant
orthologous variants: 80192235-G-C

http://identifiers.org/hco/19/GRCh38#1524050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80192296-A-C

1524062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron variant
orthologous variants: 80192308-G-T

http://identifiers.org/hco/19/GRCh38#1524214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80192469-C-A

http://identifiers.org/hco/19/GRCh38#1524272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80192557-C-A

1524272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron variant
orthologous variants: 80192557-C-T

1524283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron variant
orthologous variants: 80192578-G-A

1524283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron variant
orthologous variants: 80192578-G-T

1524333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron variant
orthologous variants: 80192630-A-G

1524380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron variant
orthologous variants: 80192683-G-A

1524525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron variant
orthologous variants: 80192930-T-C

1524637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron variant
orthologous variants: 80193115-G-T

1525177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 80193740-T-C

1525184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 80193747-G-A

1525184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 80193747-G-T

http://identifiers.org/hco/19/GRCh38#1525245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80193780-C-A

1525245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 80193780-C-T

http://identifiers.org/hco/19/GRCh38#1525301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80193814-A-C

1525301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 80193814-A-G

1525301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 80193814-A-T

http://identifiers.org/hco/19/GRCh38#1525307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80193820-C-A

1525307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, splice_region_variant
orthologous variants: 80193820-C-T

1525452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 80193971-T-C

1525455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 80193974-G-A

1525530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 80194020-G-A

1525530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 80194020-G-T

1526252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron variant
orthologous variants: 80194362-T-C

1526403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron variant
orthologous variants: 80194548-G-T

1526404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron variant
orthologous variants: 80194549-C-T

http://identifiers.org/hco/19/GRCh38#1526449-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80194586-A-C

1526449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron variant
orthologous variants: 80194586-A-G

http://identifiers.org/hco/19/GRCh38#1526513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80194648-C-A

1526513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80194648-C-G

1526513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80194648-C-T

1526514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80194649-A-G

1526514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80194649-A-T

http://identifiers.org/hco/19/GRCh38#1526628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80194763-A-C

1526628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80194763-A-G

1526628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80194763-A-T

1526630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80194765-G-A

1526630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80194765-G-T

1526655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80194923-G-A

http://identifiers.org/hco/19/GRCh38#1526674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80195047-C-A

http://identifiers.org/hco/19/GRCh38#1526711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80195083-C-A

1526711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80195083-C-G

1526711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80195083-C-T

1526782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80195154-G-A

1526782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80195154-G-T

1526912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80195253-T-A

1526912-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80195253-T-G

1527149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80195438-T-G

1527155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80195444-G-A

1527205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80195461-C-G

1527381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80195510-C-T

1527663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80195720-G-A

1527796-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80195841-T-A

1527796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80195841-T-C

1527796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80195841-T-G

http://identifiers.org/hco/19/GRCh38#1527841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80195886-C-A

1527841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80195886-C-T

http://identifiers.org/hco/19/GRCh38#1527919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80195957-C-A

1527919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80195957-C-T

1528002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 80196055-C-G

1528002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80196055-C-T

1528083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80196136-G-A

1528083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80196136-G-T

http://identifiers.org/hco/19/GRCh38#1528085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80196138-C-A

1528101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80196154-G-A

1528275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80196244-G-A

http://identifiers.org/hco/19/GRCh38#1528313-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80196285-A-C

http://identifiers.org/hco/19/GRCh38#1528346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80196318-C-A

http://identifiers.org/hco/19/GRCh38#1528786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80196413-C-A

1528786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80196413-C-T

1528923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80196545-G-A

1528923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80196545-G-C

1528923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80196545-G-T

1528962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80196584-G-A

1528962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80196584-G-T

1528966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80196588-G-A

1528966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80196588-G-T

1529015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80196645-A-G

http://identifiers.org/hco/19/GRCh38#1529030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80196666-C-A

1529030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80196666-C-T

http://identifiers.org/hco/19/GRCh38#1529039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80196675-C-A

1529039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80196675-C-T

1529076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80196695-G-A

1529076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80196695-G-T

http://identifiers.org/hco/19/GRCh38#1529101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80196725-C-A

1529101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80196725-C-G

1529101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80196725-C-T

1529207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80196791-A-G

http://identifiers.org/hco/19/GRCh38#1529318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80196895-A-C

1529318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80196895-A-G

1529318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80196895-A-T

http://identifiers.org/hco/19/GRCh38#1531706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80198807-C-A

1531706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80198807-C-T

1531710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80198811-G-A

1531710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80198811-G-T

1531955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80199068-T-C

http://identifiers.org/hco/19/GRCh38#1533837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80199968-C-A

1533837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 80199968-C-T

1533855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 80199987-G-A

1533855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 80199987-G-T

1533887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80200021-G-A

1533887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80200021-G-T

1534296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80200323-G-C

1535012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80200879-A-G

1535014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80200881-G-T

http://identifiers.org/hco/19/GRCh38#1535034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80200888-C-A

1535034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80200888-C-G

1535034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80200888-C-T

1535078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80200937-G-A

1535111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80200970-G-A

1535111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80200970-G-T

http://identifiers.org/hco/19/GRCh38#1535127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#80200986-C-A

1535127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80200986-C-T

1535133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80200992-C-T

1535222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80201087-A-G

1535261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80201116-G-A

1535261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80201116-G-C

1535261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80201116-G-T

1535278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80201133-G-A

1535278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80201133-G-C

1535369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80201238-G-A

1535440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27001
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80201302-A-T