45405172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77002338-G-A

45405172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77002338-G-T

http://identifiers.org/hco/21/GRCh38#45405187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77002324-C-A

45405187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77002324-C-G

45405187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77002324-C-T

http://identifiers.org/hco/21/GRCh38#45405211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77002302-C-A

45405211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77002302-C-T

45405216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77002297-G-A

45405216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77002297-G-T

45405256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77002266-G-A

45405256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77002266-G-C

45405256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77002266-G-T

http://identifiers.org/hco/21/GRCh38#45405307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#77002236-C-A

45405307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77002236-C-G

45405307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77002236-C-T

45405311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77002232-G-A

45405311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77002232-G-C

45405311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77002232-G-T

http://identifiers.org/hco/21/GRCh38#45405445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77002150-C-A

45405445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 77002150-C-G

45405445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 77002150-C-T

45405521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 77002065-T-C

45405612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77001966-G-T

45406111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77001341-C-T

45406225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77001225-G-A

45406225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77001225-G-T

45406342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77001107-C-T

45406557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 77000906-G-C

http://identifiers.org/hco/21/GRCh38#45406782-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77000659-A-C

45406782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 77000659-A-G

45407004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, undefined
orthologous variants: 77000484-C-G

45407334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 77000151-A-G

45407334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 77000151-A-T

45407434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77000059-T-C

http://identifiers.org/hco/21/GRCh38#45407446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77000046-C-A

http://identifiers.org/hco/21/GRCh38#45407471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#77000024-C-A

http://identifiers.org/hco/21/GRCh38#45407702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76999831-C-A

45407743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76999820-C-T

45407829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76999757-G-A

45407849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76999737-G-C

http://identifiers.org/hco/21/GRCh38#45407991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76999641-C-A

45408207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76999418-A-G

45408362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76999276-T-C

45408469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76998589-A-G

45408503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76998569-G-A

45409878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76998004-G-T

45409899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76997983-G-A

45409899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76997983-G-T

45409976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76997908-G-A

45409976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76997908-G-T

http://identifiers.org/hco/21/GRCh38#45409991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76997891-C-A

45409991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76997891-C-T

45410027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76997859-G-T

45410349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76997577-C-T

45410570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76996778-T-A

45410570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76996778-T-C

45410898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76996464-G-A

45410898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76996464-G-T

45410926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76996436-C-G

45410926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76996436-C-T

45410927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76996435-G-A

45410927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76996435-G-C

45410927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76996435-G-T

45410969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76996387-G-C

45411564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76995691-G-A

45411615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, undefined
orthologous variants: 76995641-C-T

45411638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, undefined
orthologous variants: 76995624-C-G

45411642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76995620-C-T

45411827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76995497-G-T

45412987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76994817-T-C

45413438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76994410-A-G

http://identifiers.org/hco/21/GRCh38#45413462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76994392-C-A

45413705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76994187-C-T

http://identifiers.org/hco/21/GRCh38#45413961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76993954-C-A

45413961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76993954-C-T

45414123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76993671-C-T

45414165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76993633-C-T

45414357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76993451-C-G

45414450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76993408-G-A

45416251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76991333-C-T

45416285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76991299-T-C

45420064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76987524-G-A

http://identifiers.org/hco/21/GRCh38#45420097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76987493-C-A

45420097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76987493-C-T

http://identifiers.org/hco/21/GRCh38#45420136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76987459-C-A

45420136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76987459-C-T

45420271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76987345-G-A

45420271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76987345-G-T

45420355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76987252-C-T

http://identifiers.org/hco/21/GRCh38#45420366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76987241-C-A

45420400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76987193-G-T

45420402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76987191-G-T

45420500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76987070-A-G

http://identifiers.org/hco/21/GRCh38#45420506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76987064-C-A

45420506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76987064-C-T

45420563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76987007-A-G

45420707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986829-A-G

http://identifiers.org/hco/21/GRCh38#45420709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76986827-C-A

45420709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986827-C-G

45420709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986827-C-T

http://identifiers.org/hco/21/GRCh38#45420765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76986789-C-A

45420765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986789-C-T

45420774-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986779-T-A

45420774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986779-T-C

45420791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986762-G-A

http://identifiers.org/hco/21/GRCh38#45420797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76986756-C-A

45420797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986756-C-T

45420874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986660-G-A

45420874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986660-G-T

45420877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986657-G-A

45420877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986657-G-C

45420877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986657-G-T

45420878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986656-T-C

http://identifiers.org/hco/21/GRCh38#45420900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76986631-A-C

45420900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986631-A-G

http://identifiers.org/hco/21/GRCh38#45420902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76986629-C-A

45420902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986629-C-T

http://identifiers.org/hco/21/GRCh38#45420923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76986604-C-A

45420923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986604-C-T

45420927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986600-T-C

45420951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986576-T-C

45420951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986576-T-G

45421015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986519-C-G

45421015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986519-C-T

http://identifiers.org/hco/21/GRCh38#45421095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76986433-C-A

45421095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986433-C-T

45421111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986417-T-C

45421111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986417-T-G

45421133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986386-G-A

45421133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986386-G-T

45421157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986358-A-T

45421164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986351-A-G

45421269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986160-T-C

45421270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986159-G-T

45421281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986151-G-A

45421281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986151-G-C

45421281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986151-G-T

http://identifiers.org/hco/21/GRCh38#45421282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76986150-C-A

45421305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986127-G-A

45421305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986127-G-T

45421391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986032-G-A

45421391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76986032-G-C

45427899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, undefined
orthologous variants: 76978298-A-G

45427902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, undefined
orthologous variants: 76978295-C-T

http://identifiers.org/hco/21/GRCh38#45430330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76974605-A-C

45430350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76974585-C-T

45430395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76974535-T-C

45430567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76974383-G-A

45430611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76974339-C-G

45430611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76974339-C-T

45431061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76972785-G-A

45431105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76972755-G-A

http://identifiers.org/hco/21/GRCh38#45431117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76972743-C-A

45431127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76972733-A-G

45431210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76972669-G-A

45431617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76972494-G-A

45431656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76972471-G-A

45431749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76972365-A-G

http://identifiers.org/hco/21/GRCh38#45431752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76972362-C-A

45431786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76972339-C-T

45431874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76972251-G-A

45432179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76972002-G-A

45435402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76969879-G-C

http://identifiers.org/hco/21/GRCh38#45435453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76969812-C-A

45435516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76969758-G-A

45435553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76969717-C-T

45438696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76968293-G-C

45438976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76968046-G-A

45439584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76966558-T-A

45443540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961183-T-C

45443540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961183-T-G

45443560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961163-G-C

45443571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961146-G-T

45447095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76958096-A-G

45447376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76957911-A-T

45447392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76957893-T-C

45447415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76957869-A-T

45447455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76957827-A-G

45447581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76957686-T-G

45448174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76957171-T-C

45448210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76957129-C-T

45448237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76957118-A-T

45448263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76957092-C-T

45448298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76957041-G-A

45448308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76957031-A-T

45448476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76956868-C-T

http://identifiers.org/hco/21/GRCh38#45448493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76956856-A-C

45448648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76956750-A-G

45451910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76953676-C-T

45452000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76953595-C-T

45452034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76953572-G-A

45452114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76953509-G-A

45452255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76953398-G-A

45453340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76953357-C-T

45453344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76953353-C-G

45453344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76953353-C-T

45453425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76953273-G-A

45453963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76952869-C-T

45453982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76952824-G-A

45454030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76952776-C-T

45454133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76952681-G-C

45454149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76952665-G-A

45454389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76952451-G-T

45454539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76952321-G-A

45454807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76952157-G-A

http://identifiers.org/hco/21/GRCh38#45455344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#76949676-C-A

45455344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, undefined
orthologous variants: 76949676-C-G

45455344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, undefined
orthologous variants: 76949676-C-T

http://identifiers.org/hco/21/GRCh38#45455495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76949538-C-A

45455495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76949538-C-T

45455666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant
orthologous variants: 76949349-C-T

45455769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant
orthologous variants: 76949246-C-G

45455941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 76949026-G-A

45455941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant
orthologous variants: 76949026-G-C

45455960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant
orthologous variants: 76949007-G-A

45455960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant
orthologous variants: 76949007-G-C

45455963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 76949004-C-T

http://identifiers.org/hco/21/GRCh38#45456000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76948967-C-A

45456000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant
orthologous variants: 76948967-C-T

45456111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant
orthologous variants: 76948856-C-T

45456131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant
orthologous variants: 76948836-C-T

45456150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant
orthologous variants: 76948817-G-A

45456150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant
orthologous variants: 76948817-G-C

http://identifiers.org/hco/21/GRCh38#45456259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76948690-C-A

45456259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 76948690-C-G

45456259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 76948690-C-T

45456386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant
orthologous variants: 76948539-C-G

http://identifiers.org/hco/21/GRCh38#45456492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76948439-C-A

45456492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant
orthologous variants: 76948439-C-T

45456533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 76948398-C-T

45456565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 76948366-C-T

45456636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant
orthologous variants: 76948295-G-A

45456819-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant
orthologous variants: 76948112-T-A

45456848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant
orthologous variants: 76948083-G-A

45456848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant
orthologous variants: 76948083-G-T

45457037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76947879-G-A

45457037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76947879-G-C

45457236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76947688-C-T

45457338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76947584-G-A

45458741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76947129-G-A

45459164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76946761-C-T

45459244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76946670-G-A

45459251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76946663-T-A

45459375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76946543-A-G

45459539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76946383-C-T

45460761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76945247-C-G

45466844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76933718-G-C

45466865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76933697-C-T

45468222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76932387-A-G

http://identifiers.org/hco/21/GRCh38#45468331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76932278-C-A

45468331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: synonymous variant
orthologous variants: 76932278-C-T

http://identifiers.org/hco/21/GRCh38#45468349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76932260-C-A

45468357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: synonymous variant
orthologous variants: 76932252-C-T

45468364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: 76932245-G-C

45468400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: 76932209-T-C

45468415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: synonymous variant
orthologous variants: 76932194-C-T

45468457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: synonymous variant
orthologous variants: 76932152-C-T

45468840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76931786-G-T

http://identifiers.org/hco/21/GRCh38#45468850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76931776-C-A

45468850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76931776-C-T

45468886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76931760-A-G

http://identifiers.org/hco/21/GRCh38#45468927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76931757-C-A

45468927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76931757-C-T

45469002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76931694-G-A

45469089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76931611-G-A

45469928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76930757-A-G

45470035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76930653-G-A

45470035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76930653-G-T

45470107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76930577-C-T

45470142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76930546-G-A

45470143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76930545-G-A

45470143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76930545-G-T

45470379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76930307-T-C

45471397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76929939-A-T

45471399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76929937-T-G

45471444-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76929890-T-G

45471465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76929864-G-A

45472555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76927258-T-C

http://identifiers.org/hco/21/GRCh38#45473885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76924798-C-A

45474056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76924631-A-G

45474059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76924625-G-A

45474059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76924625-G-T

http://identifiers.org/hco/21/GRCh38#45474078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76924608-C-A

45474078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76924608-C-T

45474099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76924588-T-C

45474100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76924587-G-A

45474100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76924587-G-T

45474275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76924440-G-A

45474294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76924400-T-C

45474341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76924344-A-G

http://identifiers.org/hco/21/GRCh38#45474391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76924298-A-C

45474479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76924214-C-G

45474492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76924202-G-A

45474587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76924142-T-C

http://identifiers.org/hco/21/GRCh38#45475470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76923267-C-A

45475553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76923190-G-A

45475553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76923190-G-T

http://identifiers.org/hco/21/GRCh38#45476298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76921286-C-A

45476298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76921286-C-G

http://identifiers.org/hco/21/GRCh38#45476300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76921284-A-C

45476300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76921284-A-G

http://identifiers.org/hco/21/GRCh38#45476313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76921270-C-A

45476313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76921270-C-T

45476315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76921268-G-A

http://identifiers.org/hco/21/GRCh38#45476460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76921119-C-A

45476460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: 76921119-C-T

http://identifiers.org/hco/21/GRCh38#45476462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76921117-A-C

45476462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: 76921117-A-G

45476463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: 76921116-C-T

45476493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76921087-C-T

45476522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76921061-G-A

45476522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76921061-G-T

45476557-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76921035-A-T

45476577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76921017-G-C

45476577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76921017-G-T

http://identifiers.org/hco/21/GRCh38#45476623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#76920983-C-A

45476643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76920974-A-G

45476663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76920965-G-T

45476688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76920940-A-G

45476764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76920870-G-A

45476789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76920858-G-A

45476829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76920816-G-T

45476841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76920808-G-A

45477280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76917191-G-T

45477309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76917151-G-C

45477309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76917151-G-T

45477334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76917126-G-T

45477471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: 76916997-G-A

45477501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76916967-C-T

45477535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76916939-T-C

45477547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76916927-G-T

http://identifiers.org/hco/21/GRCh38#45477573-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76916882-A-C

45477573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76916882-A-G

http://identifiers.org/hco/21/GRCh38#45477609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76916845-C-A

45477609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76916845-C-G

http://identifiers.org/hco/21/GRCh38#45477630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76916814-C-A

45477630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76916814-C-T

45477644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76916800-T-C

45477644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76916800-T-G

45477645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76916799-G-A

45477645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76916799-G-T

45477651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76916793-A-G

45477651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76916793-A-T

http://identifiers.org/hco/21/GRCh38#45477653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76916791-C-A

45477653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76916791-C-G

45477653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76916791-C-T

45477684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76916756-G-A

45477685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76916754-G-A

http://identifiers.org/hco/21/GRCh38#45477688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76916751-C-A

45477688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76916751-C-T

45477689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76916750-A-G

45477783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: 76916663-G-T

45477794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: synonymous variant
orthologous variants: 76916652-A-T

http://identifiers.org/hco/21/GRCh38#45477801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76916645-C-A

45477801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: 76916645-C-G

45477801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: 76916645-C-T

http://identifiers.org/hco/21/GRCh38#45477849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76916624-C-A

45477849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: 76916624-C-T

45477952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: 76916524-G-A

45477952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: 76916524-G-T

45477978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, undefined
orthologous variants: 76916498-G-A

45477978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, undefined
orthologous variants: 76916498-G-T

45478021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76916479-A-G

45478028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76916472-G-T

45478132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, undefined
orthologous variants: 76916360-G-T

45478140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, undefined
orthologous variants: 76916351-A-G

45478288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76915159-G-A

45478288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76915159-G-T

45478330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense_variant, undefined
orthologous variants: 76915116-G-A

45478330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense_variant, undefined
orthologous variants: 76915116-G-C

http://identifiers.org/hco/21/GRCh38#45479766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76914497-A-C

45479766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76914497-A-G

45479766-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76914497-A-T

http://identifiers.org/hco/21/GRCh38#45479776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76914484-C-A

45479776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76914484-C-T

45479779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76914481-C-T

45479839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76914421-G-A

45479839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76914421-G-T

45479983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76914268-G-A

45480080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: 76914175-G-A

45480109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: stop gained
orthologous variants: 76914155-C-T

http://identifiers.org/hco/21/GRCh38#45480145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76914119-C-A

45480145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: 76914119-C-T

45480188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76914076-G-A

45480213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76914053-A-G

http://identifiers.org/hco/21/GRCh38#45480235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76914021-C-A

45480235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76914021-C-T

http://identifiers.org/hco/21/GRCh38#45480243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76914013-C-A

45480243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76914013-C-T

45480296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76913994-G-T

45480297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76913993-G-A

45480297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76913993-G-T

45480333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76913952-G-A

45480333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76913952-G-C

45480333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76913952-G-T

45480364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76913933-T-A

45480387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76913930-G-A

45480387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76913930-G-T

45480563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76913801-C-T

http://identifiers.org/hco/21/GRCh38#45480687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76913687-C-A

45480687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76913687-C-T

http://identifiers.org/hco/21/GRCh38#45480730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76913644-C-A

45480730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: 76913644-C-T

45480887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76913487-G-A

45480887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76913487-G-T

45480890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76913484-G-A

45480890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76913484-G-T

http://identifiers.org/hco/21/GRCh38#45480924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76913450-A-C

45480924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76913450-A-G

45480924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76913450-A-T

45480954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76913416-C-T

45480986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76913404-T-A

45480986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76913404-T-C

45480986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76913404-T-G

45480989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76913401-G-A

45480989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76913401-G-T

45481034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76913368-G-C

http://identifiers.org/hco/21/GRCh38#45481956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76913060-C-A

45481956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 76913060-C-G

45481956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 76913060-C-T

45481990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: 76913026-G-A

45482005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: 76913011-A-G

http://identifiers.org/hco/21/GRCh38#45482067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76912956-C-A

45482067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76912956-C-T

45482070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76912953-A-G

45482645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76912163-A-G

45482648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76912160-G-A

45482648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76912160-G-T

45482664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76912144-A-G

http://identifiers.org/hco/21/GRCh38#45486796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76910386-C-A

45486796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76910386-C-T

45486984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: 76910190-G-A

45486984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: 76910190-G-C

45486984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: 76910190-G-T

http://identifiers.org/hco/21/GRCh38#45487010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76910164-C-A

45487010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76910164-C-T

http://identifiers.org/hco/21/GRCh38#45487037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76910122-C-A

45487037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76910122-C-G

45487037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76910122-C-T

45487075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76910071-A-G

http://identifiers.org/hco/21/GRCh38#45487322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76909752-C-A

45487322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76909752-C-T

45487352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76909721-A-G

45487372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76909699-G-A

45487372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76909699-G-C

45487372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76909699-G-T

http://identifiers.org/hco/21/GRCh38#45487472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76909609-C-A

45487602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76909523-G-A

45487602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76909523-G-T

45487757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76909420-G-C

45487757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76909420-G-T

45487814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76909402-C-G

45487836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76909380-C-T

45487917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76909295-T-C

45487917-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76909295-T-G

http://identifiers.org/hco/21/GRCh38#45487990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76909223-C-A

45487990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76909223-C-T

45488487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76908760-G-T

45488497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76908750-G-A

45488497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76908750-G-C

http://identifiers.org/hco/21/GRCh38#45488564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76908716-C-A

45488564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76908716-C-T

45488582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76908696-A-T

45488690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76908602-A-T

45488908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76908409-C-T

45489195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76908184-A-G

http://identifiers.org/hco/21/GRCh38#45489344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76908015-C-A

45489344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76908015-C-T

45489394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76907977-G-A

45489394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76907977-G-T

45489418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76907966-G-A

45489418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76907966-G-C

45489418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76907966-G-T

45489421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76907963-G-A

45489421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76907963-G-T

http://identifiers.org/hco/21/GRCh38#45489439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76907941-C-A

45489439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76907941-C-T

http://identifiers.org/hco/21/GRCh38#45489497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76907883-C-A

45489497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: synonymous variant
orthologous variants: 76907883-C-G

45489497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: synonymous variant
orthologous variants: 76907883-C-T

45489539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76907841-G-A

45489544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76907836-G-C

45489544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76907836-G-T

http://identifiers.org/hco/21/GRCh38#45489553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76907827-C-A

45489553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76907827-C-G

45489553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76907827-C-T

45489561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76907819-A-G

45489561-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76907819-A-T

45490206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76907574-T-A

http://identifiers.org/hco/21/GRCh38#45490247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76907535-C-A

45490247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76907535-C-G

45490247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76907535-C-T

45490290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: 76907492-G-A

45490290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: 76907492-G-T

http://identifiers.org/hco/21/GRCh38#45490331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76907451-C-A

45490331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: synonymous variant
orthologous variants: 76907451-C-G

45490331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: synonymous variant
orthologous variants: 76907451-C-T

http://identifiers.org/hco/21/GRCh38#45490344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76907438-C-A

http://identifiers.org/hco/21/GRCh38#45490714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76907286-C-A

45490890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76907115-G-T

http://identifiers.org/hco/21/GRCh38#45490996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76907004-C-A

45491004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76906996-T-C

45491251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: synonymous variant
orthologous variants: 76906856-G-A

http://identifiers.org/hco/21/GRCh38#45491758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76906602-C-A

45491867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76906492-G-A

45491867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76906492-G-T

45491976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76906389-G-A

45491976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76906389-G-C

45492013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76906359-C-T

45492143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76906233-G-A

45492164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76906193-G-A

45492237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76906105-C-T

http://identifiers.org/hco/21/GRCh38#45492401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76905968-C-A

45492401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76905968-C-T

45492436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76905930-T-A

45492534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: splice acceptor variant
orthologous variants: 76905812-G-T

45492550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: 76905796-G-A

45492613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76905747-A-G

45492639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76905723-C-T

45492667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76905698-C-T

45492705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: 76905660-G-C

http://identifiers.org/hco/21/GRCh38#45492742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76905622-C-A

45492742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76905622-C-T

45492751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76905595-T-G

45492763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76905583-T-A

45492763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76905583-T-C

45492833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76905535-T-A

45492858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76905510-A-G

http://identifiers.org/hco/21/GRCh38#45493104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76905393-C-A

45493109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76905386-G-A

http://identifiers.org/hco/21/GRCh38#45493175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76905318-C-A

45493175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense variant
orthologous variants: 76905318-C-T

45493558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76904239-G-A

45493558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76904239-G-T

45493710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76904159-T-A

45493710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76904159-T-C

45493710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76904159-T-G

http://identifiers.org/hco/21/GRCh38#45493754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76904116-C-A

45493754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76904116-C-T

http://identifiers.org/hco/21/GRCh38#45493756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76904114-C-A

45493756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76904114-C-T

45493770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76904097-T-A

45493770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76904097-T-C

http://identifiers.org/hco/21/GRCh38#45493780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76904087-C-A

45493780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76904087-C-T

45493860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76904047-T-A

45493860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76904047-T-C

http://identifiers.org/hco/21/GRCh38#45493898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76904011-C-A

45493898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76904011-C-T

45493930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903990-C-T

http://identifiers.org/hco/21/GRCh38#45493932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76903988-C-A

45493973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903942-G-A

45493973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903942-G-T

45493981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903934-T-C

45493981-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903934-T-G

http://identifiers.org/hco/21/GRCh38#45494007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76903897-C-A

45494007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903897-C-T

45494014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903890-C-G

45494014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903890-C-T

http://identifiers.org/hco/21/GRCh38#45494038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76903870-C-A

45494038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903870-C-T

45494050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903858-G-A

45494050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903858-G-T

45494078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903837-G-A

45494094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903821-C-T

45494100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903815-C-G

45494174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903757-A-G

http://identifiers.org/hco/21/GRCh38#45494187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76903744-C-A

http://identifiers.org/hco/21/GRCh38#45494230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76903723-A-C

45494230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903723-A-G

http://identifiers.org/hco/21/GRCh38#45494251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76903694-A-C

45494305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903648-A-G

45494305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903648-A-T

http://identifiers.org/hco/21/GRCh38#45494307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76903646-C-A

45494307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903646-C-G

http://identifiers.org/hco/21/GRCh38#45494369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76903596-C-A

45494369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903596-C-T

45494376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903591-C-G

45494376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903591-C-T

45494475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903551-G-A

45494591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903450-T-A

45494591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903450-T-C

45494700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903397-T-G

http://identifiers.org/hco/21/GRCh38#45494734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76903363-C-A

45494734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903363-C-G

45494734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903363-C-T

45494745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903355-T-A

45494759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903343-G-T

45494768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903334-G-A

45494768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903334-G-T

http://identifiers.org/hco/21/GRCh38#45494774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76903328-C-A

45494774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903328-C-T

http://identifiers.org/hco/21/GRCh38#45494784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76903318-C-A

45494788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903314-T-C

45494796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903306-G-A

45494796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903306-G-C

45494796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903306-G-T

http://identifiers.org/hco/21/GRCh38#45494798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76903300-C-A

45494798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903300-C-T

45494847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903278-C-G

45494847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903278-C-T

http://identifiers.org/hco/21/GRCh38#45494933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76903193-C-A

http://identifiers.org/hco/21/GRCh38#45494984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76903161-C-A

45494984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903161-C-T

45494987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903158-G-A

45494987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903158-G-C

45494987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903158-G-T

http://identifiers.org/hco/21/GRCh38#45495087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76903063-C-A

45495087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903063-C-T

45495133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903021-G-A

45495133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903021-G-C

45495133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76903021-G-T

45495164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76902986-C-T

45495206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76902955-G-T

45495211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76902950-G-A

45495211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76902950-G-T

45495213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76902948-G-A

45495213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76902948-G-T

45495225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76902934-T-A

45495225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76902934-T-C

45495240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76902918-T-C

45495240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76902918-T-G

45495241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76902917-G-A

45495241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76902917-G-C

45495241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76902917-G-T

45495242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76902916-T-A

45495242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76902916-T-C

45495248-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76902910-T-A

45495248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76902910-T-C

45495321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76902891-G-A

45495321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76902891-G-T

45495499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76902715-G-A

45495499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76902715-G-T

45495549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76902672-A-T

45495573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76902649-G-A

45495573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76902649-G-T

http://identifiers.org/hco/21/GRCh38#45495587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76902634-C-A

45495587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76902634-C-T

http://identifiers.org/hco/21/GRCh38#45495600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76902620-C-A

http://identifiers.org/hco/21/GRCh38#45495621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76902605-C-A

45495621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76902605-C-T

45496364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 76901271-G-A

45496455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76901186-T-C

http://identifiers.org/hco/21/GRCh38#45496597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76901053-C-A

45496597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76901053-C-T

45496606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76901044-T-A

45496606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76901044-T-C

45496606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76901044-T-G

45496609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76901041-G-A

45496877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76900808-C-T

45496905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76900780-C-G

45496905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76900780-C-T

45496909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76900765-T-G

45497006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76900473-T-C

http://identifiers.org/hco/21/GRCh38#45497140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76900312-C-A

45497140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76900312-C-T

45497238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76900220-G-A

45497238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76900220-G-T

45497292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76900124-G-C

45497484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76899978-T-G

45497572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76899898-A-G

45497572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76899898-A-T

45497766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76899713-G-A

45497766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76899713-G-T

http://identifiers.org/hco/21/GRCh38#45497778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76899701-C-A

45497778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76899701-C-G

45497778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76899701-C-T

http://identifiers.org/hco/21/GRCh38#45497808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76899672-C-A

45497808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76899672-C-T

45502207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76897098-G-A

45502213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76897092-G-A

45502393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76896929-G-T

45502438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76896885-G-C

http://identifiers.org/hco/21/GRCh38#45502716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76896683-C-A

45502716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76896683-C-T

45502913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76896552-G-A

45502913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76896552-G-T

45502942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76896524-G-A

45503858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76896417-G-A

45503858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76896417-G-C

45503858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76896417-G-T

45503883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76896391-A-G

45503937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76896351-G-A

45504043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76896212-G-T

http://identifiers.org/hco/21/GRCh38#45504122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76896139-A-C

45504122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76896139-A-G

45504246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895992-G-A

45504246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895992-G-T

45504270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895969-G-A

45504270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895969-G-C

45504270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895969-G-T

45504304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895954-G-A

45504304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895954-G-T

http://identifiers.org/hco/21/GRCh38#45504506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76895759-C-A

45504506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant
orthologous variants: 76895759-C-T

http://identifiers.org/hco/21/GRCh38#45504509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76895756-C-A

45504509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant
orthologous variants: 76895756-C-G

45504509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant
orthologous variants: 76895756-C-T

http://identifiers.org/hco/21/GRCh38#45504565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76895718-C-A

45504565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895718-C-T

http://identifiers.org/hco/21/GRCh38#45504606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76895661-C-A

45504606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895661-C-T

http://identifiers.org/hco/21/GRCh38#45504642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76895637-C-A

45504642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895637-C-T

http://identifiers.org/hco/21/GRCh38#45504661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76895617-C-A

45504661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895617-C-T

45504668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895610-A-G

45504693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895577-T-C

45504705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895565-G-A

45504705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895565-G-T

45504744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895543-C-T

45504823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895481-C-T

45504840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895464-A-G

45504842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895462-G-C

45504863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895437-A-G

45504919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895389-A-T

45504941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895365-C-T

http://identifiers.org/hco/21/GRCh38#45505035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76895297-C-A

45505035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895297-C-T

45505113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895251-G-A

45505113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895251-G-C

45505113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895251-G-T

45505284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895084-T-C

45505284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895084-T-G

45505285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 76895083-C-T

45505292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895076-G-T

http://identifiers.org/hco/21/GRCh38#45505313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76895053-C-A

45505313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895053-C-T

45505314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895052-G-A

http://identifiers.org/hco/21/GRCh38#45505318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76895048-C-A

45505318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895048-C-G

45505318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895048-C-T

45505326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76895040-T-A

45505570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76894899-G-A

45505570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76894899-G-T

45505575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76894894-G-A

45505575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76894894-G-T

45505630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76894865-G-A

45505733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron variant
orthologous variants: 76894744-G-T

45505889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant
orthologous variants: 76894608-C-T

45505913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant
orthologous variants: 76894584-G-A

45505913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant
orthologous variants: 76894584-G-T

45507582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76893212-C-T

http://identifiers.org/hco/21/GRCh38#45507600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76893194-A-C

45507600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 76893194-A-G

45509288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76891734-G-C

45509288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76891734-G-T

45509299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76891717-G-A

45509299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76891717-G-T

http://identifiers.org/hco/21/GRCh38#45509339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76891677-A-C

45509413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76891602-T-A

45509413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76891602-T-C

http://identifiers.org/hco/21/GRCh38#45509428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76891587-C-A

45509428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76891587-C-T

45509496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76891519-G-A

45509496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76891519-G-T

http://identifiers.org/hco/21/GRCh38#45509509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76891506-C-A

45509509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76891506-C-T

45509602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 76891410-G-A

45509602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 76891410-G-T

45509623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76891391-G-A

45509623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76891391-G-C

45509623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76891391-G-T

45509625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76891389-T-C

45509673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76891344-C-T

http://identifiers.org/hco/21/GRCh38#45509816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76891182-C-A

45509867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76891078-G-A

http://identifiers.org/hco/21/GRCh38#45509950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76890925-A-C

45509950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76890925-A-G

45510018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76890867-G-A

45510018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76890867-G-T

http://identifiers.org/hco/21/GRCh38#45510040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76890845-C-A

45510040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76890845-C-T

http://identifiers.org/hco/21/GRCh38#45510088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76890789-C-A

45510088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76890789-C-T

45510187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76890690-T-A

45510199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 76890678-C-T

45510214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76890663-A-G

http://identifiers.org/hco/21/GRCh38#45510247-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76890630-A-C

45510247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76890630-A-G

45510247-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76890630-A-T

http://identifiers.org/hco/21/GRCh38#45510408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76890534-C-A

45510408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76890534-C-G

45510409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76890533-T-C

45510454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76890503-C-T

http://identifiers.org/hco/21/GRCh38#45510455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76890502-C-A

45510474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76890489-C-T

45510517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76890456-C-T

http://identifiers.org/hco/21/GRCh38#45510549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76890428-A-C

45510667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76890348-A-G

45510740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76890286-T-C

45511099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76890114-T-C

45511099-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76890114-T-G

http://identifiers.org/hco/21/GRCh38#45511163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76890050-C-A

45511163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76890050-C-T

45511272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889965-G-A

45511273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889964-G-A

45511273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889964-G-T

45511304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889936-T-A

45511304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889936-T-G

45511412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889868-C-T

45511477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889837-G-A

45511541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889792-G-A

45511622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889721-T-C

45511765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889555-G-C

45511781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889539-T-G

45511825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889518-C-G

45511847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889498-A-G

45511891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889457-G-A

45511891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889457-G-C

45511942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889410-T-C

45512106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889295-T-C

45512170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889256-G-A

45512189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 76889238-C-T

http://identifiers.org/hco/21/GRCh38#45512261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76889166-C-A

45512261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76889166-C-T

45512268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76889159-A-T

45512333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76889094-G-A

45512333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76889094-G-C

45512333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76889094-G-T

http://identifiers.org/hco/21/GRCh38#45512342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76889085-C-A

45512342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76889085-C-T

45512426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76888997-A-G

45512458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76888974-G-A

45512458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76888974-G-T

45512492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76888945-G-A

45512492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76888945-G-C

45512492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76888945-G-T

http://identifiers.org/hco/21/GRCh38#45512586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76888849-A-C

45512586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76888849-A-G

45512664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76888797-G-A

45512667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76888784-T-C

45512692-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76888759-T-A

45512692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76888759-T-C

http://identifiers.org/hco/21/GRCh38#45512694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76888757-A-C

45512695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76888756-T-A

45512695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76888756-T-C

http://identifiers.org/hco/21/GRCh38#45512706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76888745-C-A

45512706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76888745-C-T

45512712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76888739-T-C

45512712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76888739-T-G

http://identifiers.org/hco/21/GRCh38#45512716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76888735-C-A

http://identifiers.org/hco/21/GRCh38#45512773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76888691-C-A

http://identifiers.org/hco/21/GRCh38#45512821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76888646-C-A

45512821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76888646-C-T

http://identifiers.org/hco/21/GRCh38#45512827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76888640-C-A

45512827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76888640-C-T

45512891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76888577-T-A

45512891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76888577-T-G

45512907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76888568-G-A

45512907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76888568-G-T

http://identifiers.org/hco/21/GRCh38#45512974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76888479-C-A

45512974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76888479-C-T

45513139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76888387-G-A

45513140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76888386-C-T

45513243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76888348-G-A

45513243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76888348-G-T

http://identifiers.org/hco/21/GRCh38#45513291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#76888337-C-A

45513291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76888337-C-T

45513550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2195
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76888191-T-C