http://identifiers.org/hco/13/GRCh38#46553186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75185260-C-A

46553186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75185260-C-T

46553232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75185216-G-A

46553232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75185216-G-C

46553232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75185216-G-T

http://identifiers.org/hco/13/GRCh38#46553272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75185199-C-A

46553272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75185199-C-T

46553384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75185111-G-A

46553384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75185111-G-C

46553384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75185111-G-T

http://identifiers.org/hco/13/GRCh38#46553499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75184993-C-A

46553499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75184993-C-T

46553518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 75184974-C-T

http://identifiers.org/hco/13/GRCh38#46553520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75184972-C-A

46553712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75184813-G-A

46553712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75184813-G-C

46553836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75184756-G-A

46553836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75184756-G-T

46553902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75184691-C-G

46553902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75184691-C-T

http://identifiers.org/hco/13/GRCh38#46554055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75184600-A-C

46554331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75184373-A-G

46554791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75183975-A-G

46554791-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75183975-A-T

46555255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75183512-A-G

46555316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75183474-T-C

46555691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75183088-T-C

46555702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75183076-G-C

46555767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75182996-G-A

46556607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75182124-A-G

46556826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75181919-T-C

http://identifiers.org/hco/13/GRCh38#46556836-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75181909-A-C

http://identifiers.org/hco/13/GRCh38#46557057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75181738-C-A

46557182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75181620-G-T

46557206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75181596-G-A

46557206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75181596-G-T

46558346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75180582-G-A

http://identifiers.org/hco/13/GRCh38#46558389-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75180543-A-C

46559004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75180250-G-A

46559097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75180147-T-A

46559398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75179290-T-C

46559501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75179169-C-T

46559632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75179051-A-G

http://identifiers.org/hco/13/GRCh38#46560180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75178570-A-C

46560180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75178570-A-T

46560512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75177716-G-A

46560588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75177546-T-C

46560614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75177512-C-T

46560970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75176937-T-G

46561326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75175972-T-A

46561373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75175922-T-G

46561630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75175704-G-A

46561778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75175559-T-C

http://identifiers.org/hco/13/GRCh38#46561890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75175447-A-C

46563074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75174084-C-G

46564027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75171701-T-C

46564148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75171580-G-T

46564184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75171544-G-A

46564318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75171417-G-A

46564356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75171379-A-G

46564812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75170263-G-A

46564812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75170263-G-T

46564840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75170243-G-A

46564901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75170174-C-T

46564916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75170158-A-G

46565046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75170051-A-G

46565099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75169999-T-C

46565167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75169930-G-A

46565195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75169908-A-G

http://identifiers.org/hco/13/GRCh38#46565277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75169825-C-A

http://identifiers.org/hco/13/GRCh38#46565311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75169790-A-C

46565311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75169790-A-G

46565420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75169717-C-T

46566024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75169489-G-T

46566026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75169487-G-C

46567157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75168672-G-A

46567175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75168651-T-C

46567826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75167027-G-A

46568698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75165398-A-G

46568770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75165266-G-T

46568774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75165262-A-G

46568855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75165194-A-G

46569051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75165013-G-A

46569192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75164892-G-C

46569391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75164721-A-G

46569721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75164386-G-A

46569752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75164355-G-A

46569752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75164355-G-C

46569819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75164287-C-T

46570120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75163969-C-G

46570237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75163873-G-A

46570348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75163785-G-C

46570490-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75163670-T-G

46570519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75163642-A-G

46570546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75163608-C-T

46571761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75161857-T-A

46572083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75161678-C-T

46572516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75161296-A-G

46575474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75160728-A-G

46575491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75160710-C-T

46578827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75159502-G-T

46578867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75159465-C-G

http://identifiers.org/hco/13/GRCh38#46578876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75159416-C-A

46578876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75159416-C-T

46579352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75158986-A-G

46579353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75158985-C-T

46579367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75158971-C-T

46579523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75158379-C-G

46579528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75158374-T-C

46579579-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75158319-T-A

46579660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75158236-C-T

46579687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75158216-C-T

46580075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75157867-C-G

46580150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75157791-T-A

46584928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75156809-G-A

46585995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75156098-G-T

46586089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75156018-C-T

46586229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75155897-G-A

46586937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75155408-G-A

46586938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75155407-C-T

46587589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75154784-G-C

46587965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75153594-G-A

46588199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75153386-T-G

46588373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75153213-G-A

http://identifiers.org/hco/13/GRCh38#46590079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75152431-A-C

46590124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75152389-G-T

46590140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75152373-G-A

46590253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75152248-A-G

46590260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75152241-G-A

46590292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75152218-A-G

46590713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75151611-A-G

46590727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75151597-T-C

46590904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75151435-T-C

46591104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75151287-C-T

46591331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75151046-T-G

46591615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75150082-C-T

46591870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75149851-A-G

46591932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75149810-G-A

46591932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75149810-G-T

46592008-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75149733-A-T

http://identifiers.org/hco/13/GRCh38#46592350-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75149323-A-C

46592403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75149267-C-G

46592426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75149243-A-G

http://identifiers.org/hco/13/GRCh38#46592632-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75149067-A-C

46592632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75149067-A-T

46593374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75148255-G-A

46593386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75148243-A-G

http://identifiers.org/hco/13/GRCh38#46595468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75146708-C-A

46595468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75146708-C-G

46595468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75146708-C-T

46595797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75146382-T-C

http://identifiers.org/hco/13/GRCh38#46595885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75146307-A-C

46595885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75146307-A-T

46595890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75146302-A-T

46596342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75145493-A-G

46596342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75145493-A-T

46596541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75145283-A-G

46596737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75145108-T-C

46596944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75144920-T-C

46596944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75144920-T-G

http://identifiers.org/hco/13/GRCh38#46597103-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75144758-A-C

46597280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75144586-T-A

46597328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75144543-C-G

46597690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75144495-A-T

46597993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75144227-T-C

46598301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75143973-C-T

46598357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75143925-A-G

46598658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75143651-C-T

46598764-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75143545-T-G

46598881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75143323-A-G

46599059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75143131-A-G

46600187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75142760-A-G

http://identifiers.org/hco/13/GRCh38#46600199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75142748-A-C

46600199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75142748-A-G

46600233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75142715-T-C

46600281-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75142675-T-A

46600355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75142607-A-G

46600410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75142551-G-A

46600441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75142522-T-C

46600448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75142515-C-G

46600448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75142515-C-T

46600465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75142498-C-T

46602036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75141589-C-T

46602325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75141405-T-C

46602400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75141333-A-G

46602548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75141171-C-T

46602655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75141067-G-T

46602994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75140955-A-G

46604585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75137999-G-A

46604742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75137862-T-C

46605016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75137692-T-C

http://identifiers.org/hco/13/GRCh38#46605372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75137374-C-A

46605372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75137374-C-G

46605372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75137374-C-T

46605590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75137138-T-A

http://identifiers.org/hco/13/GRCh38#46605660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75137072-A-C

46605807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75136914-A-G

46605926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75136823-G-A

46606178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75136610-G-T

46606338-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75136441-A-T

46606448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75136358-G-C

46607330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75135848-T-G

46607559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75135659-G-A

46607562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75135656-C-T

46608042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75134156-G-T

46608178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75131716-A-G

46608233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75131671-G-A

46608296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75131602-A-G

46608301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75131597-A-G

46608381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75131528-G-A

46608661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75131330-G-C

46608661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75131330-G-T

46614030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75130493-C-T

46614086-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75130466-A-T

46614115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75130424-T-C

46614116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75130423-T-C

46614121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75130406-T-G

http://identifiers.org/hco/13/GRCh38#46614254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75130271-A-C

46614367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75129685-T-C

46614435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75129626-T-G

46614543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75129523-A-G

46614803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75129256-G-A

46615740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75128409-G-A

46615776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75128379-C-T

http://identifiers.org/hco/13/GRCh38#46615992-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75128174-A-C

46616096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75128079-C-G

46616275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75127904-T-C

46616301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75127878-T-A

46616301-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75127878-T-G

46616447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75127727-C-T

46616646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75127542-A-G

46616646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75127542-A-T

46616675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75127514-C-G

46617211-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75127019-T-G

46617216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75127014-A-G

46617259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75126972-G-A

46617789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75126504-A-G

46617811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75126482-C-G

46617827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75126469-T-C

46618522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75126202-G-A

46618585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75126143-G-A

46619573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75125492-A-G

46620051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75125075-T-C

46620080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75125046-G-A

46620206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75124881-C-T

46620579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75124445-G-A

46620689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75124339-A-G

46621281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75123744-C-T

46621340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75123701-T-C

46621429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75123631-A-G

46621440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75123620-T-C

46621630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75123462-C-G

46621992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75123128-A-G

46622041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75123083-A-G

46622233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75122743-G-T

46622320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75122651-A-G

46622715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75122252-G-T

46622836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75122138-T-C

46622996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75121985-G-A

46623009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75121972-G-A

46623278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75121687-T-C

46624098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75120954-G-A

46624137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75120927-G-A

46624361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75120744-G-A

46624620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75120540-G-A

46626027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75118249-A-G

46626691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75118005-A-G

46626694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75118002-T-A

46626694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75118002-T-C

46626698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75117998-C-T

46627579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75117260-T-C

http://identifiers.org/hco/13/GRCh38#46627601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75117225-C-A

46627641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75117187-C-T

46627821-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75117025-T-A

46627840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75117006-T-G

46628060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75116889-G-T

http://identifiers.org/hco/13/GRCh38#46628099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75116852-C-A

46628234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75116591-G-C

46629382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75116027-G-A

46629520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75115900-G-T

46629621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75115793-C-T

46630645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75115541-G-A

46630699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75115490-G-C

46630997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75115180-C-G

46630997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75115180-C-T

http://identifiers.org/hco/13/GRCh38#46631023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75115154-C-A

46631023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75115154-C-T

46631370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75114776-A-G

46631495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75114652-A-G

46631661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75114478-A-G

46631694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75114449-A-G

46631780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75114026-G-A

46631999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75113722-C-T

http://identifiers.org/hco/13/GRCh38#46632371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75113392-A-C

46632384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75113379-T-C

46632392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75113371-C-T

46632854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75112886-C-T

46633270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75112454-C-T

46633291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75112428-T-C

46633563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75112157-A-G

46633687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75112058-C-T

http://identifiers.org/hco/13/GRCh38#46633832-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75111908-A-C

46633848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75111896-C-T

46634444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75111645-C-T

46634838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75111240-G-A

46635056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75110997-A-G

46635081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75110968-G-T

46637272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75109296-T-A

46637442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75109159-C-T

46637455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75109154-G-A

46637456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75109153-G-A

46637457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75109152-C-T

46637491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75109117-G-A

46637602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75109006-C-T

46637623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75108985-T-C

46637652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75108974-G-A

46637779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75108882-G-T

46638071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75108544-C-T

46638219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75108235-T-C

46638472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75108003-T-C

http://identifiers.org/hco/13/GRCh38#46638664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75107820-C-A

46638664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75107820-C-T

46639820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75107561-T-C

46639973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75107423-C-T

46639980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75107416-C-T

46640251-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75106875-A-T

46640252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75106874-T-C

46640259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75106867-A-T

46640287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75106840-C-G

46640287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75106840-C-T

46640298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75106829-A-G

46640673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75106580-T-G

46640716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75106552-A-G

46640988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75106356-T-C

http://identifiers.org/hco/13/GRCh38#46641103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75106276-C-A

46641103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75106276-C-T

46641196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75106172-A-G

46641876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75105151-G-C

46642307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75104745-C-T

46642471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75104626-C-T

http://identifiers.org/hco/13/GRCh38#46642579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75104273-C-A

46642689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75104160-G-A

46643507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75102732-C-T

46643508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75102731-A-T

46643640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75102639-A-G

http://identifiers.org/hco/13/GRCh38#46643645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75102634-C-A

46643645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75102634-C-G

46644080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75102334-G-A

46644312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75101948-C-G

http://identifiers.org/hco/13/GRCh38#46650371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75095387-C-A

http://identifiers.org/hco/13/GRCh38#46650517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75095252-A-C

46650518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75095251-C-G

46650578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75095185-G-T

46650615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75095152-G-T

46650678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75095089-T-A

46650684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75095083-A-G

46650744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75095041-A-G

46650744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75095041-A-T

46650769-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75095020-T-A

46650800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75094978-A-G

46651046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75094687-T-C

46651162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75094589-C-T

46651178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75094578-C-G

46651180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75094576-C-T

46651328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75094390-T-C

46651328-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75094390-T-G

46651365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75094355-G-A

46652406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75094303-T-G

46652411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75094298-G-T

46652425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75094284-C-G

46652470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75094220-G-A

46652515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75094175-T-C

46652522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75094168-T-C

46652538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75094152-T-C

46652538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75094152-T-G

46652612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75094098-G-A

46652726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75093985-G-T

46652765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75093949-G-A

46652779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75093935-A-G

46652791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75093923-T-C

http://identifiers.org/hco/13/GRCh38#46652810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75093907-C-A

46652972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75093777-C-G

46653414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75093160-G-A

46653415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75093159-A-T

46653956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75092434-G-A

46654950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75091559-G-A

46655427-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75091055-T-G

46655811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75090706-A-G

46655855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75090665-G-A

46656002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75090522-A-G

http://identifiers.org/hco/13/GRCh38#46656045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75090479-C-A

46656076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75090448-G-A

46656076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75090448-G-T

46656111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75090413-C-T

46656242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75090262-A-G

46656328-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75090205-T-G

46656417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75090126-A-G

46656581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75089899-T-C

46657253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75089260-G-T

46658036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75088313-G-A

46658212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75088173-T-C

46658248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75088160-A-G

46658278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75088135-T-C

46659522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75086640-C-G

46659567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75086597-A-G

46659691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75086509-G-C

46659691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75086509-G-T

46659964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75086258-G-C

46660379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75086151-G-A

http://identifiers.org/hco/13/GRCh38#46660399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75086131-C-A

46660399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75086131-C-T

46660624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75085791-T-C

46660682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75085733-C-T

46660860-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75085554-T-G

46660883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75085530-C-T

46660965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75085067-G-A

46662491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75084540-T-G

46663072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75083991-T-C

46663168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75083887-C-T

http://identifiers.org/hco/13/GRCh38#46663318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75083711-C-A

http://identifiers.org/hco/13/GRCh38#46663407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75083601-C-A

46663407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75083601-C-T

http://identifiers.org/hco/13/GRCh38#46663669-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75083357-A-C

46664008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75083074-T-A

46665065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75082142-T-C

46665112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75082099-T-C

46665827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75078657-C-T

46666357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75078037-C-T

46666471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75077853-C-T

46666472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75077852-G-A

46666472-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75077852-G-C

46666516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75077831-A-G

46666627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75077738-A-G

46666832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75077415-C-T

46667068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75077237-G-A

46667209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75077103-G-A

46667283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75077064-C-T

46667308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75077039-A-G

46667316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75077031-A-G

46667316-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75077031-A-T

46667331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75077016-T-G

46667803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75076822-T-C

46667803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75076822-T-G

46667865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75076762-G-C

46668216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75076459-A-G

46668510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75076187-T-C

46668982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75073261-G-T

46669082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75073161-G-A

46673347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75071512-G-C

46673755-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75071068-T-G

46674379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75070724-A-G

46674560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75070553-T-C

46674764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75070364-T-C

46675021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75070142-G-T

46675141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75069363-G-A

46675198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75069307-G-A

46675198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75069307-G-T

46675341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75069159-G-T

46675513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75069016-G-A

46675517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75069012-A-G

46675654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75068878-G-A

46675698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75068844-C-G

46675698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75068844-C-T

46675821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75068726-C-T

46675915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75068638-G-A

46675915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75068638-G-C

46675956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75068595-A-G

46676322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75068511-A-G

46676387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75068464-T-A

46677916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75067785-T-C

46677935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75067766-G-A

46677935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75067766-G-C

46678024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75067677-T-C

46678170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75067529-G-A

46678379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75067328-T-C

46678482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75067218-A-G

46678631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75067104-A-G

46678721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75067014-G-T

46678728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75067007-T-C

46678760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75066974-C-T

46678761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75066973-G-A

46678948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75066758-T-G

http://identifiers.org/hco/13/GRCh38#46679135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75066580-C-A

46679135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75066580-C-G

46679155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75066560-T-C

46679180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75066539-C-T

46679203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75066518-A-G

46679243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75066476-C-G

46679357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75066352-A-G

46679377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75066332-C-T

46679673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75066137-G-C

46679732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75066079-A-T

46679806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75066004-T-C

http://identifiers.org/hco/13/GRCh38#46679813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75065997-C-A

46679813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75065997-C-T

46679815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75065995-A-G

46679816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75065994-G-C

46679816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75065994-G-T

46679844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75065968-G-A

46679844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75065968-G-T

46679848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75065964-C-G

46679852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75065960-T-A

46679852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75065960-T-C

46679905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75065934-G-T

46679941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75065903-G-T

46679967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75065878-T-C

46679978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75065861-A-G

46680308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75065498-G-A

46680386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75065433-A-T

46680420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75065402-A-T

46680466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75065362-G-C

46680576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75065261-A-T

46680649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75065175-G-A

46680686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75065138-G-C

46680757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75065088-G-A

http://identifiers.org/hco/13/GRCh38#46680847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75065013-C-A

46680847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75065013-C-T

46680933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75064886-G-T

46680972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75064849-C-T

http://identifiers.org/hco/13/GRCh38#46681088-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75064747-A-C

46681173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75064647-C-T

46681250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75064584-G-A

46681271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75064563-A-G

46681466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75064401-G-A

46681492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75064382-G-A

46681493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75064381-G-T

46681550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75064338-C-T

http://identifiers.org/hco/13/GRCh38#46681611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75064278-C-A

46681611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75064278-C-T

46681670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75064228-G-A

46681700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75064205-G-A

46681700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75064205-G-T

46681854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75064028-A-G

46681864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75064020-A-G

46681868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75064016-T-C

46681868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75064016-T-G

46681922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75063974-A-T

46682004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75063870-T-C

46682048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75063827-C-T

46682240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75063695-C-G

46682240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75063695-C-T

46682244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75063691-G-C

http://identifiers.org/hco/13/GRCh38#46682692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75063266-C-A

46682692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75063266-C-G

46682756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75063222-T-C

46682832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75063157-C-T

46683287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75060475-G-A

46683777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75059980-T-C

46683951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75059768-C-T

46684022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75059696-G-A

46684069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75059654-C-T

46684232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75059503-C-T

46684813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75058159-A-G

46684880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75058088-C-G

46684880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75058088-C-T

46685090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75057877-G-A

46685386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75057583-C-T

46685498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75057455-A-G

46685518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75057434-A-T

46685564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75057392-G-T

46685565-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75057391-T-G

46685701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75057288-T-C

46685722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75057267-T-C

46685722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75057267-T-G

46685745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75057240-T-C

46685748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75057237-A-G

46685761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75057224-A-G

http://identifiers.org/hco/13/GRCh38#46685767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75057218-A-C

46685767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75057218-A-G

46685837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75057142-A-G

http://identifiers.org/hco/13/GRCh38#46685907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75057066-C-A

46685907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 75057066-C-G

46685907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 75057066-C-T

http://identifiers.org/hco/13/GRCh38#46685916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75057057-C-A

46685916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75057057-C-T

46686033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75056940-C-T

46687573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75056310-A-G

46687739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75056167-G-A

46687739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75056167-G-C

46687739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75056167-G-T

http://identifiers.org/hco/13/GRCh38#46687755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75056151-A-C

46687755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75056151-A-T

46687756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75056150-A-G

46687793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75056114-T-C

http://identifiers.org/hco/13/GRCh38#46687834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75056075-C-A

46687834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75056075-C-T

46688002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75055903-G-T

http://identifiers.org/hco/13/GRCh38#46688003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75055902-C-A

46688003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75055902-C-G

http://identifiers.org/hco/13/GRCh38#46688006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75055899-C-A

46688006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75055899-C-G

http://identifiers.org/hco/13/GRCh38#46688007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75055898-A-C

46688007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75055898-A-G

46688107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75055844-A-G

http://identifiers.org/hco/13/GRCh38#46688122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75055834-C-A

http://identifiers.org/hco/13/GRCh38#46688125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75055831-C-A

46688132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75055824-G-C

46688260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75055697-T-C

46688465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75055238-A-G

46688732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75054944-A-G

46688756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75054923-A-G

46689005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75054718-G-T

46689006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75054717-C-T

46689029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75054680-G-A

46689230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75054474-A-G

http://identifiers.org/hco/13/GRCh38#46689269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75054439-C-A

46689269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75054439-C-G

46689466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75054278-A-G

46689636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75054123-G-A

46690163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75053272-G-A

46690254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75052818-C-G

46690402-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75052656-T-A

46690419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75052639-C-T

46690699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75052369-A-G

46691124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75051984-A-G

46691125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75051983-C-T

http://identifiers.org/hco/13/GRCh38#46691299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75051810-A-C

46691412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75051696-G-A

46691427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75051681-G-A

46692253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75051390-A-T

46692275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75051359-C-T

http://identifiers.org/hco/13/GRCh38#46692326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75051300-C-A

http://identifiers.org/hco/13/GRCh38#46692337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75051289-C-A

46692398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75051265-A-G

46692398-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75051265-A-T

46692406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75051257-T-G

46692456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75051212-G-A

46692456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75051212-G-T

46692492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75051195-G-T

46692542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75051143-G-A

http://identifiers.org/hco/13/GRCh38#46692551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75051134-A-C

46692551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75051134-A-G

46692566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75051119-G-A

46692566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75051119-G-T

46692633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75051052-C-T

46692649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75051036-A-T

http://identifiers.org/hco/13/GRCh38#46692714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75050976-C-A

46693162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75050724-G-T

46693274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75050642-G-C

46693343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75050602-A-G

http://identifiers.org/hco/13/GRCh38#46693357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75050588-C-A

46693357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75050588-C-G

46693378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75050569-A-G

46693514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75050428-A-T

46694067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75050016-T-A

46694129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75049954-T-C

46694231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75049832-G-A

46694270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75049795-G-A

http://identifiers.org/hco/13/GRCh38#46694790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75049259-A-C

46694790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75049259-A-G

46694799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75049247-A-G

46694803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75049243-G-T

46694835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75049213-T-C

46694848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75049200-T-C

http://identifiers.org/hco/13/GRCh38#46694878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75049168-A-C

46694878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75049168-A-G

46694926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75049132-C-T

46694941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75049117-G-A

46695109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75048962-T-C

http://identifiers.org/hco/13/GRCh38#46695124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75048940-C-A

46695124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75048940-C-T

46695128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75048936-A-G

http://identifiers.org/hco/13/GRCh38#46695150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75048917-C-A

46695154-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75048913-T-A

46695154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75048913-T-C

http://identifiers.org/hco/13/GRCh38#46695246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75048800-C-A

46695391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75048637-G-A

46695831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75048251-A-G

46695955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75048119-C-T

46696013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75048070-T-C

46696062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75048010-G-T

46696194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75047890-G-A

http://identifiers.org/hco/13/GRCh38#46696247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75047861-C-A

46696351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75047758-G-A

46697144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75047421-T-C

46697278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75047277-A-G

46697323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75047236-A-G

46697739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75046410-C-T

46697988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75046205-G-A

46698054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75046147-A-G

http://identifiers.org/hco/13/GRCh38#46698179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75046058-C-A

46698230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75046026-A-T

46698243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75046013-T-C

46698371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75045909-G-A

46698376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75045904-A-G

46698484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75045802-G-A

46698504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75045782-C-T

46698953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75045294-C-T

46698959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75045288-C-T

46699206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75045088-G-A

46699264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75045030-G-C

http://identifiers.org/hco/13/GRCh38#46699270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75045023-C-A

http://identifiers.org/hco/13/GRCh38#46699331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75044984-C-A

46699341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75044974-G-A

46699341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75044974-G-C

46699465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75044861-G-A

46699465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75044861-G-T

46699490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75044837-A-G

46699490-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75044837-A-T

46699504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75044823-G-T

46699536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75044790-T-G

46699567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75044765-C-T

46699659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75044598-A-T

46699738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75044275-C-G

46699793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75044225-A-G

46699951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75044074-A-T

46700056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75043959-C-T

46700091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75043924-A-G

46700163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75043855-A-G

46700206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75043812-G-T

46700261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75043747-A-G

46700326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75043679-G-A

46700429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75043587-G-A

46700966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75043127-C-T

46700979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75043114-A-G

46701029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75043064-G-A

46701029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75043064-G-T

46701143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75042968-G-A

46701158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75042953-A-G

46701204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75042910-A-G

46701229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75042883-A-G

46701281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75042824-T-C

46701287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75042818-A-G

http://identifiers.org/hco/13/GRCh38#46701297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75042808-C-A

46701297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75042808-C-G

46701306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75042799-T-C

46701318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75042787-A-G

46701377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75042731-G-A

46701650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75042495-A-G

46701695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75042449-G-T

46704891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75042040-T-C

http://identifiers.org/hco/13/GRCh38#46704962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75041984-C-A

46704995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75041955-A-G

http://identifiers.org/hco/13/GRCh38#46705002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75041948-C-A

46705008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75041942-G-T

46705034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75041922-A-G

46705073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75041883-G-A

http://identifiers.org/hco/13/GRCh38#46705074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75041882-C-A

46705107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75041849-A-G

46705235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75041725-T-A

46705235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75041725-T-C

http://identifiers.org/hco/13/GRCh38#46705263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75041700-C-A

46705263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75041700-C-T

46705454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75041564-G-T

http://identifiers.org/hco/13/GRCh38#46705503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75041521-C-A

46705503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75041521-C-T

46705616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75041382-G-A

46705616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75041382-G-T

http://identifiers.org/hco/13/GRCh38#46705631-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75041367-A-C

46705712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75041302-G-A

46705712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75041302-G-T

46705819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75040956-C-T

46705838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75040937-G-A

46706116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75038558-G-A

http://identifiers.org/hco/13/GRCh38#46706180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75038499-C-A

46706180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75038499-C-T

46706239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75038444-T-C

46706479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75038217-T-G

46707434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75036569-C-T

46707446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75036557-A-G

46707471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75036532-T-C

46707489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75036514-G-A

46707489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75036514-G-C

46707495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75036508-A-G

46707506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75036497-G-A

http://identifiers.org/hco/13/GRCh38#46708023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75035662-A-C

46709641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75035189-G-A

46709714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75035109-A-G

46709788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75035048-C-T

46710036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75034879-T-G

46710156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75034778-G-A

46710393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75034587-C-T

46710483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75034505-T-C

46710630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75034395-T-C

46710671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75034358-T-C

46710773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75034282-A-G

46711015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75034133-C-T

46711345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75033960-A-G

46711389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75033910-T-C

46711389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75033910-T-G

46711410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75033900-C-G

46711483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75033826-C-G

46711559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75033756-A-G

46711597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75033720-G-T

http://identifiers.org/hco/13/GRCh38#46711687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75033631-C-A

46711687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75033631-C-T

46711746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75033570-T-C

46711784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 75033536-T-C

46711800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: missense variant
orthologous variants: 75033520-G-A

46711800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: missense variant
orthologous variants: 75033520-G-C

46711903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75033417-T-A

46711931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75033391-T-C

46711933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75033388-G-T

46712154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75033175-G-C

46712154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75033175-G-T

46712288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75033036-A-G

46712413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75032896-G-A

46712413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75032896-G-T

46712428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75032881-G-A

46712429-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75032880-T-A

46712429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75032880-T-G

http://identifiers.org/hco/13/GRCh38#46712669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75032672-C-A

http://identifiers.org/hco/13/GRCh38#46712688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75032656-C-A

46712688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75032656-C-T

46712689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75032655-T-C

http://identifiers.org/hco/13/GRCh38#46712701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75032643-C-A

46712701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75032643-C-T

46712720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75032616-T-C

46712720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75032616-T-G

46712746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75032590-G-T

46712777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75032568-C-G

46712777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75032568-C-T

46712801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75032544-A-G

46713286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75032080-T-G

46713305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75032061-T-G

http://identifiers.org/hco/13/GRCh38#46713445-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75031926-A-C

http://identifiers.org/hco/13/GRCh38#46713548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75031825-A-C

46713564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75031809-T-A

46713656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75031669-C-T

46713712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75031556-G-A

46713883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75031444-A-G

46713900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75031428-A-G

46715152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75031072-G-A

46715152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75031072-G-T

46715161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75031063-A-G

46715446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75030778-T-C

46715687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75030542-T-A

46715687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75030542-T-C

http://identifiers.org/hco/13/GRCh38#46715709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75030521-C-A

46715718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75030512-T-C

46715773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75030457-G-A

46715773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75030457-G-T

46715874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75030364-A-G

46715917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75030322-C-G

46716720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75030081-G-C

46716816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75029762-G-A

46717246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75029310-C-T

46717313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75029247-A-G

46717426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75029132-G-A

46717426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75029132-G-T

46717435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75029123-G-A

46717435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75029123-G-T

46717448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75029110-G-T

46717714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75028817-A-G

46717865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75028666-T-G

46717897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75028625-A-G

46717954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75028569-A-G

46717961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75028562-G-A

46718103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75028435-T-C

46718181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75028356-A-G

46718462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75028139-G-T

http://identifiers.org/hco/13/GRCh38#46718506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75028107-C-A

46718637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75027974-A-G

46718656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75027956-T-C

46718807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75027817-T-C

46718807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75027817-T-G

46719125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75027566-T-G

46719225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75027463-A-G

46719247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75027441-A-G

46720794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75026889-C-T

46720820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75026886-T-A

http://identifiers.org/hco/13/GRCh38#46720975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75026783-C-A

46720975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75026783-C-G

46721134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75026622-C-T

46721438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75026280-T-A

46721625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75026107-A-G

46721805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75025935-C-T

46721822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75025917-G-A

46721838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75025910-T-A

46721880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75025876-A-G

46722004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75025792-C-G

46722004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75025792-C-T

46722151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75025671-A-G

http://identifiers.org/hco/13/GRCh38#46722201-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75025627-A-C

46722224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75025601-C-G

46722299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75025519-G-A

46722524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75024423-T-C

46722533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75024414-T-C

46722540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75024408-G-A

46722547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75024401-C-T

46722972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75024069-C-T

46723005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75024036-A-G

46723083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75023955-G-A

46723104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75023934-T-C

http://identifiers.org/hco/13/GRCh38#46723206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75023843-C-A

46723206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75023843-C-T

46723358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75023692-G-A

http://identifiers.org/hco/13/GRCh38#46723380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75023663-C-A

46723380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75023663-C-G

46723401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75023642-G-A

46723408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75023631-T-A

46723408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75023631-T-C

http://identifiers.org/hco/13/GRCh38#46723414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75023625-C-A

46723414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75023625-C-T

http://identifiers.org/hco/13/GRCh38#46723419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75023620-C-A

46723419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75023620-C-G

46728765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75023132-T-G

http://identifiers.org/hco/13/GRCh38#46728767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75023130-C-A

46728767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75023130-C-G

46728767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75023130-C-T

http://identifiers.org/hco/13/GRCh38#46728840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75023073-C-A

46728840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 75023073-C-T

46728935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: missense variant
orthologous variants: 75022978-A-G

46728943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: missense_variant, undefined
orthologous variants: 75022970-C-G

46728952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: missense variant
orthologous variants: 75022961-G-A

46728952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: missense variant
orthologous variants: 75022961-G-T

http://identifiers.org/hco/13/GRCh38#46729054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75022864-A-C

46729073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75022845-G-A

46729073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75022845-G-T

http://identifiers.org/hco/13/GRCh38#46729100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75022814-C-A

http://identifiers.org/hco/13/GRCh38#46729101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75022813-C-A

46729101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75022813-C-G

46729101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75022813-C-T

46729115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75022801-A-G

46729115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75022801-A-T

46729130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75022786-G-A

46729130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75022786-G-C

46729157-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75022768-T-A

46730011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75022231-A-G

46730050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75022195-G-A

46730146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75022101-G-T

46730184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75022064-T-C

46730184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75022064-T-G

46730290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75021949-A-G

46730405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75021840-G-C

46730431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75021824-G-A

46732034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75014192-G-A

46733514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75013360-C-T

46734015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75013002-T-C

46734025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75012992-T-C

46734053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75012967-T-C

46734143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75012870-A-G

46734233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75012768-A-G

http://identifiers.org/hco/13/GRCh38#46734369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75012682-C-A

46734590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75012473-T-G

46734644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75012423-C-T

46734661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75012407-G-T

46734737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75012352-G-T

46734823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75012266-T-C

46734857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75012195-C-T

46735134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75011960-C-T

http://identifiers.org/hco/13/GRCh38#46735202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75011883-C-A

46735259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75011824-G-A

46735280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75011805-C-G

46735280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75011805-C-T

46735300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75011791-A-G

46735337-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75011754-A-T

46735482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75011641-A-G

46735622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75011516-A-G

46735756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75011410-A-G

46736927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75011173-G-A

46737017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75011087-A-G

46737632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75010630-C-G

46737762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75010505-A-G

46738030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75010277-A-G

46738160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75010189-C-T

46738171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75010178-A-T

46738172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75010177-G-T

http://identifiers.org/hco/13/GRCh38#46738177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75010172-C-A

46738357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75009988-A-G

46738423-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75009942-T-G

46738585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75009805-G-A

46738617-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75009778-T-G

46738806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75009576-A-G

46738950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75008943-A-G

46739484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75005133-T-C

46739852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75004772-A-G

46740030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75004521-T-G

46740112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75004448-C-T

46740125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75004435-G-C

46740256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75004295-G-A

46740908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75003335-C-G

46741274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75003043-A-G

46741369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75002923-T-C

46741442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75002856-C-T

46741523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75002802-G-A

46741523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 75002802-G-C

http://identifiers.org/hco/13/GRCh38#46741738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75002589-C-A

46741857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75002470-C-T

46741974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75002352-G-C

46741974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75002352-G-T

46741976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75002350-A-G

46742041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75002280-T-G

46742080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75002241-G-A

46742214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75002110-G-A

46742214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75002110-G-T

46742247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75002090-A-G

46742277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75002061-G-A

46742277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75002061-G-T

http://identifiers.org/hco/13/GRCh38#46742351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75001993-C-A

46742351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75001993-C-G

46742351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75001993-C-T

46742554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75001796-T-C

46742554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75001796-T-G

46742621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75001741-T-C

46742657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75001706-G-A

46742657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75001706-G-T

46742720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75001643-G-A

46742720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75001643-G-C

46742720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75001643-G-T

http://identifiers.org/hco/13/GRCh38#46742743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75001620-C-A

46742743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75001620-C-G

46742759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75001606-A-G

46742792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75001573-T-C

46742802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75001561-G-C

46742842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75001524-T-C

46742928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75001434-A-G

46742930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75001430-C-T

46742984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75001376-C-T

46743003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75001355-G-C

46743003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75001355-G-T

46743040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75001315-G-T

46743123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75001227-C-G

46743186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75001164-A-G

46743188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75001162-C-T

46743266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75001084-G-T

http://identifiers.org/hco/13/GRCh38#46743285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75001065-A-C

46743355-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75000990-T-G

46743637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75000716-G-C

46743726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75000625-G-A

46743750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75000605-A-G

46743755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75000600-C-T

46743796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75000547-G-A

46743801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75000542-C-G

46743801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75000542-C-T

46743906-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75000474-T-A

46743911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75000469-G-A

46743914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75000466-C-T

46744068-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75000318-T-G

46744127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75000256-C-G

http://identifiers.org/hco/13/GRCh38#46744150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75000234-A-C

46744451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74999963-A-G

46744552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74999869-A-G

46744552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74999869-A-T

http://identifiers.org/hco/13/GRCh38#46744743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#74999706-A-C

46744783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74999652-G-A

46744903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74999521-G-A

http://identifiers.org/hco/13/GRCh38#46744961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#74999481-A-C

46745390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74999061-G-C

46745390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74999061-G-T

46745441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74999018-G-A

46745441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74999018-G-T

http://identifiers.org/hco/13/GRCh38#46745464-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#74998997-A-C

46745482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74998984-G-A

46745681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74998864-G-A

46745775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74998762-C-G

46745791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74998745-A-G

http://identifiers.org/hco/13/GRCh38#46745863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#74998664-C-A

46746100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74998612-T-G

46746118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74998594-T-C

http://identifiers.org/hco/13/GRCh38#46746125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#74998587-C-A

46746125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74998587-C-T

http://identifiers.org/hco/13/GRCh38#46746150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#74998561-A-C

46746169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74998551-G-A

46746189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74998535-C-T

46746296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74998485-G-C

46746405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74998392-A-G

46746453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74998344-G-T

46746554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74998246-G-A

46746970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74997927-G-A

46746971-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74997926-A-T

46746980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74997918-C-T

46747034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74997864-A-G

46747113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74997792-G-C

46748347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74996833-G-T

46748350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74996830-T-A

46748392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74996786-A-G

http://identifiers.org/hco/13/GRCh38#46748614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#74996574-A-C

http://identifiers.org/hco/13/GRCh38#46748730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#74996464-C-A

46748730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74996464-C-T

46748741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74996453-A-G

46748773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74996422-T-C

46748829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74996389-G-C

46748973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74996231-A-G

46749243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74995962-G-A

46749260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74995945-T-C

46750223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74994889-T-G

46750336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74994776-A-G

http://identifiers.org/hco/13/GRCh38#46750358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#74994757-C-A

46750358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74994757-C-T

http://identifiers.org/hco/13/GRCh38#46750400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#74994715-A-C

46750413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74994701-G-T

46750422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74994692-G-T

46750456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74994661-T-G

46750493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74994629-A-G

46750496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74994626-G-C

46750516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: intron variant
orthologous variants: 74994605-A-G

http://identifiers.org/hco/13/GRCh38#46750656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#74994465-C-A

46750656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: 74994465-C-T

http://identifiers.org/hco/13/GRCh38#46750720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#74994399-C-A

46750771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: 74994343-A-G

http://identifiers.org/hco/13/GRCh38#46750915-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#74994211-A-C

46750915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: 74994211-A-G

http://identifiers.org/hco/13/GRCh38#46750972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#74994155-C-A

46750972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: 74994155-C-T

http://identifiers.org/hco/13/GRCh38#46750987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#74994140-A-C

46750987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: 74994140-A-G

46751038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: 74994085-G-A

46751038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: 74994085-G-T

46751521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: 74993566-G-A

http://identifiers.org/hco/13/GRCh38#46751535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#74993553-C-A

46751658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: 74993431-G-C

46751678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: 74993410-T-C

46751893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: 74993241-G-A

46752000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: 74993123-G-T

46752065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 74993059-A-G

46752104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: 74993020-G-C

46752104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: 74993020-G-T

46752186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 74992922-C-G

46752213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: 74992891-T-A

46752221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: 74992883-T-C

46752301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: 74992804-G-A

46752318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: 74992787-G-T

46752329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: 74992779-A-G

46752389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: 74992732-C-T

46752437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: 74992705-G-A

46752454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: 74992688-G-A

46752454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: 74992688-G-T

46752572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: 74992577-G-A

46752582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20309
most severe consequence: 3 prime UTR variant
orthologous variants: 74992567-G-A