http://identifiers.org/hco/16/GRCh38#57512269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95629447-C-A

57512269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 3 prime UTR variant
orthologous variants: 95629447-C-T

57512276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 3 prime UTR variant
orthologous variants: 95629454-A-G

57512280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 3 prime UTR variant
orthologous variants: 95629458-G-A

57512400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95629585-G-A

57512400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95629585-G-T

57512425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95629611-G-C

57512436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95629622-T-G

57512509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95629678-G-A

57512509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95629678-G-T

57512571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95629719-C-T

http://identifiers.org/hco/16/GRCh38#57512591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95629739-C-A

57512593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95629741-G-A

57512593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95629741-G-C

57512593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95629741-G-T

http://identifiers.org/hco/16/GRCh38#57512600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95629744-C-A

57512602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95629746-A-G

57512640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95629785-G-T

57512849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95629998-G-A

57512849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95629998-G-C

57512911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95630059-G-A

57512911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95630059-G-T

57512930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95630072-G-T

http://identifiers.org/hco/16/GRCh38#57512935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95630077-C-A

57512935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95630077-C-T

57512992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95630096-T-C

57513004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95630103-A-G

57513141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95630235-G-A

57513162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95630255-T-C

57513371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95630374-A-T

57513374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95630377-T-A

57513377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95630380-T-C

57513463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95630452-G-A

57513463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95630452-G-C

57513876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95630878-C-T

57514602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95631090-G-A

57514602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95631090-G-C

57514602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95631090-G-T

57514689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95631156-C-G

57514689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95631156-C-T

57514902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95631358-C-T

http://identifiers.org/hco/16/GRCh38#57515251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95631799-C-A

57515251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95631799-C-G

57515251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95631799-C-T

57515285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95631834-G-C

57515285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95631834-G-T

57515286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95631835-A-G

http://identifiers.org/hco/16/GRCh38#57515482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95632023-C-A

57515482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95632023-C-T

http://identifiers.org/hco/16/GRCh38#57515606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95632067-C-A

57515728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95632103-C-T

57516035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95632339-T-C

http://identifiers.org/hco/16/GRCh38#57516161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95632461-C-A

57516161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95632461-C-G

57516218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95632510-G-A

57516218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95632510-G-T

57516260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95632552-C-T

http://identifiers.org/hco/16/GRCh38#57516419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95632686-C-A

57516419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95632686-C-T

http://identifiers.org/hco/16/GRCh38#57516443-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95632710-A-C

http://identifiers.org/hco/16/GRCh38#57516458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95632725-C-A

57516458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95632725-C-T

http://identifiers.org/hco/16/GRCh38#57516509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95632762-C-A

57516606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95632825-G-C

57516606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95632825-G-T

57516608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95632827-A-G

57516627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95632846-C-T

57516657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95632876-A-G

http://identifiers.org/hco/16/GRCh38#57516693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95632902-C-A

57516693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95632902-C-G

http://identifiers.org/hco/16/GRCh38#57516695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95632904-C-A

57516779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95632987-G-A

57517010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95633174-T-C

57517040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95633197-C-T

57517051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95633208-T-C

57517105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95633246-C-T

57517108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95633251-C-T

57517110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95633253-C-T

57517619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95633896-C-T

57518176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous variant
orthologous variants: 95634451-T-C

http://identifiers.org/hco/16/GRCh38#57518182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95634457-C-A

57518182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous variant
orthologous variants: 95634457-C-T

57518319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95634608-G-A

57518319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95634608-G-T

57518511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95634805-G-A

57518511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95634805-G-T

57518517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95634811-G-A

57518517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95634811-G-T

57518523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95634817-A-G

57518562-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95634856-T-A

57518562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95634856-T-G

http://identifiers.org/hco/16/GRCh38#57518721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95634998-C-A

57518721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous variant
orthologous variants: 95634998-C-T

57518770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, undefined
orthologous variants: 95635047-G-A

57518770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, undefined
orthologous variants: 95635047-G-T

57518808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, undefined
orthologous variants: 95635085-G-A

57518808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, undefined
orthologous variants: 95635085-G-T

http://identifiers.org/hco/16/GRCh38#57519117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95635184-C-A

57519432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95635293-T-C

57519618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95635403-G-A

57520989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95636289-T-C

http://identifiers.org/hco/16/GRCh38#57521007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95636310-C-A

57521007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95636310-C-T

57521022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95636325-G-A

57521022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95636325-G-T

57521045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95636348-A-G

57525875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95638028-G-A

57525975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous variant
orthologous variants: 95638130-C-T

http://identifiers.org/hco/16/GRCh38#57526065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95638220-C-A

57526065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous variant
orthologous variants: 95638220-C-T

57526080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous variant
orthologous variants: 95638235-A-G

57526080-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous variant
orthologous variants: 95638235-A-T

http://identifiers.org/hco/16/GRCh38#57526086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95638241-C-A

57526086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous variant
orthologous variants: 95638241-C-T

57526163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95638333-G-A

57526163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95638333-G-T

57526206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95638387-T-G

57526257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95638431-G-A

57526257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95638431-G-T

57528148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95639278-C-G

http://identifiers.org/hco/16/GRCh38#57528352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95639466-C-A

57528478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, undefined
orthologous variants: 95639588-T-A

57528478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, undefined
orthologous variants: 95639588-T-C

http://identifiers.org/hco/16/GRCh38#57528585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#95639693-C-A

57528585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 95639693-C-G

57528585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 95639693-C-T

http://identifiers.org/hco/16/GRCh38#57528611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#95639729-C-A

57528611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: missense_variant, undefined
orthologous variants: 95639729-C-G

57528611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous_variant, undefined
orthologous variants: 95639729-C-T

57528665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous_variant, undefined
orthologous variants: 95639783-G-A

57528665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous_variant, undefined
orthologous variants: 95639783-G-C

57528665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous_variant, undefined
orthologous variants: 95639783-G-T

57528713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous_variant, undefined
orthologous variants: 95639831-G-A

57528713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous_variant, undefined
orthologous variants: 95639831-G-C

57528713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous_variant, undefined
orthologous variants: 95639831-G-T

57528728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous_variant, undefined
orthologous variants: 95639846-G-A

57528728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: missense_variant, undefined
orthologous variants: 95639846-G-C

57528728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: stop_gained, undefined
orthologous variants: 95639846-G-T

57528755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous_variant, undefined
orthologous variants: 95639873-G-A

57528755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous_variant, undefined
orthologous variants: 95639873-G-T

http://identifiers.org/hco/16/GRCh38#57528767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#95639885-C-A

57528767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous_variant, undefined
orthologous variants: 95639885-C-G

57528767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous_variant, undefined
orthologous variants: 95639885-C-T

http://identifiers.org/hco/16/GRCh38#57528923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95640041-C-A

57528923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous variant
orthologous variants: 95640041-C-G

57528923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous variant
orthologous variants: 95640041-C-T

57528962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous variant
orthologous variants: 95640080-G-A

57528962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous variant
orthologous variants: 95640080-G-C

57528962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous variant
orthologous variants: 95640080-G-T

http://identifiers.org/hco/16/GRCh38#57528998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95640116-C-A

57528998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous variant
orthologous variants: 95640116-C-G

57528998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous variant
orthologous variants: 95640116-C-T

http://identifiers.org/hco/16/GRCh38#57529007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95640122-C-A

57529007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous variant
orthologous variants: 95640122-C-G

57529007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous variant
orthologous variants: 95640122-C-T

57529019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous variant
orthologous variants: 95640134-G-A

57529019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: synonymous variant
orthologous variants: 95640134-G-T

57529076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 95640191-A-G

57529142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 95640257-G-A

57529142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 95640257-G-T

57529204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 5 prime UTR variant
orthologous variants: 95640319-G-A

57529204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 5 prime UTR variant
orthologous variants: 95640319-G-C

57529204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 5 prime UTR variant
orthologous variants: 95640319-G-T

57529275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 95640391-C-G

57529275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 95640391-C-T

http://identifiers.org/hco/16/GRCh38#57529282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95640398-C-A

http://identifiers.org/hco/16/GRCh38#57529285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95640401-C-A

57529285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 95640401-C-G

57529285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 95640401-C-T

57529311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 95640423-A-G

57529388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 95640503-A-G

57529403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 95640521-G-A

57529425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95640544-A-G

57532112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95640681-G-T

57532160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95640729-C-G

57532257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95640844-C-T

57532266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95640870-C-T

57532364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95641010-T-C

57532456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95641078-T-C

57532607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95641210-C-G

57532716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95641293-C-G

57532952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95641482-G-A

57533008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95641534-G-C

57533049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95641584-G-A

57533089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95641624-G-A

57534436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95642480-G-A

57534841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95643107-G-T

57534867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95643133-G-A

57534910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95643182-C-T

57535014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95643278-C-T

57535017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95643281-G-A

57535632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95643692-G-C

57535862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, undefined
orthologous variants: 95643910-G-A

57535862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, undefined
orthologous variants: 95643910-G-C

57535906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95643997-C-T

57536099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95644239-T-C

57536210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95644350-C-G

http://identifiers.org/hco/16/GRCh38#57536211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95644351-C-A

57536211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95644351-C-G

57536272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95644408-C-T

57536287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95644411-G-A

57536325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95644458-G-A

57536365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95644495-G-A

57536365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95644495-G-C

57536365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95644495-G-T

http://identifiers.org/hco/16/GRCh38#57536421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#95644539-C-A

57536421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron_variant, undefined
orthologous variants: 95644539-C-T

57536442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95644560-G-A

http://identifiers.org/hco/16/GRCh38#57536453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95644571-C-A

57536453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95644571-C-T

57536455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95644572-G-A

57536455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95644572-G-T

http://identifiers.org/hco/16/GRCh38#57536472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95644589-C-A

57536472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: intron variant
orthologous variants: 95644589-C-T

57536508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 95644618-G-A

57536508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 95644618-G-C

57536508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 95644618-G-T

http://identifiers.org/hco/16/GRCh38#57536554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#95644661-C-A

57536554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 95644661-C-T

http://identifiers.org/hco/16/GRCh38#57536568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#95644676-C-A

57536568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 95644676-C-T

57536999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28097
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 95644975-G-A