http://identifiers.org/hco/9/GRCh38#6532528-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30075903-A-C

6532528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30075903-A-T

6532600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30075967-G-C

6532713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30076077-A-G

6532795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30076169-G-T

http://identifiers.org/hco/9/GRCh38#6532831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30076188-C-A

6532831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30076188-C-G

6532908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30076260-G-A

6532908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30076260-G-C

6532908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30076260-G-T

6532933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30076285-G-T

6532993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30076344-T-A

6533003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30076354-T-C

6533009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30076359-A-G

6533071-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30076421-T-A

http://identifiers.org/hco/9/GRCh38#6533110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30076460-A-C

6533110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30076460-A-G

6533189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30076535-T-G

http://identifiers.org/hco/9/GRCh38#6533209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30076551-C-A

6533209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30076551-C-G

6533209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30076551-C-T

6533220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30076566-A-G

6533229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30076575-G-T

6533230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30076576-C-T

6534470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30076977-G-C

6534470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30076977-G-T

6534597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30077110-A-G

6534601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30077114-T-G

6534631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30077141-G-C

6534631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30077141-G-T

6534663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30077181-G-A

http://identifiers.org/hco/9/GRCh38#6534677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30077207-C-A

6534677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30077207-C-T

http://identifiers.org/hco/9/GRCh38#6534738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30077267-A-C

http://identifiers.org/hco/9/GRCh38#6534831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30077362-C-A

6534831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30077362-C-T

http://identifiers.org/hco/9/GRCh38#6534857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30077392-C-A

6535656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30077758-A-G

6535718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30077830-C-T

http://identifiers.org/hco/9/GRCh38#6535782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30077891-C-A

6535816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30077898-A-G

http://identifiers.org/hco/9/GRCh38#6535870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30077997-C-A

6535870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30077997-C-T

6535871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30077998-A-G

6535893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30078021-G-A

6535986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30078095-G-A

6535986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30078095-G-C

6535986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30078095-G-T

http://identifiers.org/hco/9/GRCh38#6536059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30078138-C-A

6536059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30078138-C-G

6536059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30078138-C-T

6540029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30080357-A-G

6540041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30080369-A-G

6540042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30080370-G-C

6540042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30080370-G-T

6540043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30080371-C-T

6540155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30080483-G-T

6540156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30080484-A-G

6540156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30080484-A-T

http://identifiers.org/hco/9/GRCh38#6540173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30080499-A-C

6540201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30080524-A-T

6540205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30080528-A-G

6540299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30080607-G-T

6540302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30080610-A-G

http://identifiers.org/hco/9/GRCh38#6540370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30080639-C-A

6540370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30080639-C-G

6540370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30080639-C-T

6540383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30080652-A-G

6540417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30080698-G-A

6540417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30080698-G-T

6540480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30080757-T-C

6540487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30080764-T-A

6540487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30080764-T-C

6540498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30080775-G-A

http://identifiers.org/hco/9/GRCh38#6540518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30080788-C-A

6540518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30080788-C-G

6540518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30080788-C-T

http://identifiers.org/hco/9/GRCh38#6540523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30080793-C-A

http://identifiers.org/hco/9/GRCh38#6540555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30080877-C-A

6540555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30080877-C-G

6540555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30080877-C-T

6540559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30080894-T-C

6540559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30080894-T-G

6540560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30080895-T-C

6540560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30080895-T-G

6540564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30080899-G-A

6540564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30080899-G-T

http://identifiers.org/hco/9/GRCh38#6540647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30080980-C-A

6540703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30081038-A-G

6540721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30081056-G-A

6540721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30081056-G-C

6541383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30082140-C-G

6541383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30082140-C-T

6541482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30082219-T-G

http://identifiers.org/hco/9/GRCh38#6541499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30082234-C-A

6542557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30082368-T-C

http://identifiers.org/hco/9/GRCh38#6543879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30083087-C-A

6543893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30083101-G-A

6543893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30083101-G-C

6543893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30083101-G-T

6544307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30084117-C-G

http://identifiers.org/hco/9/GRCh38#6548244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30086589-A-C

6548445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30086761-G-T

6548446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30086762-C-T

http://identifiers.org/hco/9/GRCh38#6548458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30086781-A-C

6548549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30086868-C-T

http://identifiers.org/hco/9/GRCh38#6548567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30086886-A-C

6549696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30087347-G-T

http://identifiers.org/hco/9/GRCh38#6549838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30087463-C-A

6549838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30087463-C-G

6549838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30087463-C-T

6549859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30087483-G-A

6549859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30087483-G-T

6550010-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30087618-T-A

6550020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30087630-C-G

6550029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30087638-G-C

6550229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30087817-T-C

6550276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30087865-G-A

6550660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30087913-T-C

http://identifiers.org/hco/9/GRCh38#6550730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30087978-A-C

http://identifiers.org/hco/9/GRCh38#6550747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30087995-A-C

6550747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30087995-A-T

6550765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30088007-A-G

6550782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30088052-T-C

6550787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30088057-T-A

6550787-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30088057-T-G

6550864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30088134-A-G

6550906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30088176-T-C

6550968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30088237-G-A

6550968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30088237-G-T

6551022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30088288-G-A

6551022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30088288-G-T

6551214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30088689-G-A

6551214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30088689-G-C

6551214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30088689-G-T

6551411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30088899-G-T

6551707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30089119-A-G

6551729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30089141-G-C

http://identifiers.org/hco/9/GRCh38#6551784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30089190-C-A

6552260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30089562-C-T

6552334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30089636-C-T

http://identifiers.org/hco/9/GRCh38#6552357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30089659-C-A

6552357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30089659-C-G

6552357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30089659-C-T

6552465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30089770-T-A

6552577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30090414-C-T

6552787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30090618-G-A

6552792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30090624-T-C

6552831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30090670-A-G

6552836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30090675-G-A

6552836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30090675-G-T

6552911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30090745-T-C

http://identifiers.org/hco/9/GRCh38#6552930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30090762-C-A

6552975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30090802-T-C

6553055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30090882-G-A

6553189-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30090974-T-A

6553189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30090974-T-C

6553189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30090974-T-G

6553237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30091022-A-G

6553248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30091033-A-T

http://identifiers.org/hco/9/GRCh38#6553256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30091041-C-A

6553256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30091041-C-G

6553256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30091041-C-T

6553269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30091054-T-G

http://identifiers.org/hco/9/GRCh38#6553349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30091104-A-C

6553349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30091104-A-G

6553389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30091143-G-A

6553389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30091143-G-C

6553495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30091249-G-A

6553495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30091249-G-T

6553526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30091280-T-C

6553527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30091281-G-A

6553647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30091380-A-G

6553647-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30091380-A-T

6553705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30091505-C-T

6553927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30091710-G-C

6553931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30091713-T-G

6554084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30091822-G-A

6554143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30091851-T-C

6554143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30091851-T-G

http://identifiers.org/hco/9/GRCh38#6554184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30091890-C-A

6554259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30091991-T-C

6554301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30092245-A-G

6554305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30092249-G-A

6554305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30092249-G-C

6554305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30092249-G-T

6554388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30092331-G-A

6554440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30092367-G-A

6554440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30092367-G-C

6554548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30092471-G-A

6554548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30092471-G-C

6554548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30092471-G-T

6554584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30092507-A-T

6554587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30092510-T-C

6554587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30092510-T-G

6554620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30092539-C-T

6554634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30092553-C-T

6554639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30092558-C-G

6554692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30092611-A-G

6554695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30092614-A-G

6554698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30092617-T-A

6554698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30092617-T-C

6554698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30092617-T-G

http://identifiers.org/hco/9/GRCh38#6554785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30092704-C-A

6554785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30092704-C-T

6554837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30092740-G-C

6554837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30092740-G-T

6554838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30092741-T-A

6554838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30092741-T-C

6554884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30092785-A-G

6554884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30092785-A-T

6554908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30092808-T-C

http://identifiers.org/hco/9/GRCh38#6554935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30092845-C-A

6554935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30092845-C-T

http://identifiers.org/hco/9/GRCh38#6554962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30093042-C-A

6554962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30093042-C-T

6554989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30093069-A-G

http://identifiers.org/hco/9/GRCh38#6554997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30093077-A-C

6555036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30093116-G-A

6555036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30093116-G-T

6555158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30093232-C-T

6555194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30093275-A-G

http://identifiers.org/hco/9/GRCh38#6555321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30093365-C-A

6555346-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30093390-T-A

6555417-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30093433-T-G

http://identifiers.org/hco/9/GRCh38#6556110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30093770-A-C

6556110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30093770-A-G

6556110-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30093770-A-T

6556128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30093787-A-G

6556198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30093844-T-A

6556198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30093844-T-C

6556225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30093871-G-C

6556240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30093886-C-G

6556240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30093886-C-T

6556305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30093951-G-A

6556305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30093951-G-C

6556324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30093958-G-T

6556336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30093970-G-A

6556336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30093970-G-C

6556336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30093970-G-T

6556369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30094025-G-A

6556369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30094025-G-C

6556369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30094025-G-T

6556410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30094066-T-G

6556466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30094114-C-G

http://identifiers.org/hco/9/GRCh38#6556789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30094341-A-C

6556857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30094356-T-A

6556884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30094383-T-C

http://identifiers.org/hco/9/GRCh38#6556979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30094486-C-A

http://identifiers.org/hco/9/GRCh38#6556987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30094494-A-C

6557703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30094972-A-G

6557703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30094972-A-T

http://identifiers.org/hco/9/GRCh38#6557746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30095021-C-A

6557753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30095028-A-T

6557768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30095043-G-C

6557924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30095182-T-G

http://identifiers.org/hco/9/GRCh38#6557970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30095227-A-C

6557970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30095227-A-G

6558009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30095263-G-T

http://identifiers.org/hco/9/GRCh38#6558053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30095307-C-A

http://identifiers.org/hco/9/GRCh38#6558073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30095327-C-A

6558073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30095327-C-G

6558073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30095327-C-T

http://identifiers.org/hco/9/GRCh38#6558159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30095416-C-A

6558159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30095416-C-T

6558160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30095417-A-G

6558161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30095418-T-C

6558167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30095424-G-A

6558167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30095424-G-C

6558167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30095424-G-T

6558169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30095426-C-T

http://identifiers.org/hco/9/GRCh38#6558314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30095528-C-A

6558385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30095597-G-A

6558385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30095597-G-C

6558385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30095597-G-T

6558413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30095641-G-A

6558413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30095641-G-T

6558415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30095643-G-A

6558415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30095643-G-T

6558426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30095654-T-C

6558426-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30095654-T-G

6558457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30095788-T-C

6558505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30095842-C-G

6558537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30095921-C-T

6558553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 30095937-A-G

6558628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30096012-T-A

6558652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30096036-G-A

6558805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30096202-G-A

6558805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30096202-G-T

6558811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30096208-T-A

6558811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30096208-T-C

6558812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30096209-A-G

6558823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30096220-A-G

6558909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30096300-T-C

http://identifiers.org/hco/9/GRCh38#6558960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30096321-C-A

6558986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30096347-G-C

6559052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30096409-C-T

6559115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30096469-T-C

6559162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30096513-G-A

6559217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30096564-T-C

6561677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30098460-G-C

6561763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30098550-G-A

6561917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30098674-T-C

6561941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30098696-G-C

6561941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30098696-G-T

6561968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30098718-A-G

6561984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30098734-T-C

6561985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30098735-T-C

6561985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30098735-T-G

6562092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30098804-C-T

6562161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30098851-T-C

6562181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30098866-A-G

6562220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30098904-A-G

6562294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30098976-G-A

6562361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30099040-G-A

6562361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30099040-G-C

6562408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30099055-C-G

6562409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30099056-C-T

6562443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30099090-C-T

6562667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30099166-C-T

6562826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30099183-G-T

6562957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30099286-C-G

6562987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30099313-C-T

6563286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30099579-G-C

http://identifiers.org/hco/9/GRCh38#6563383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30099880-C-A

6563485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30099971-C-T

6563522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30100006-G-A

6563528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30100012-C-T

6563566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30100044-T-C

6563566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30100044-T-G

6563783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30100240-A-G

6563972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30100560-G-A

http://identifiers.org/hco/9/GRCh38#6563982-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30100572-A-C

6564108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30100828-C-T

6564109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30100829-G-A

6564201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30100930-T-A

6564201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30100930-T-C

6564272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30101138-C-T

http://identifiers.org/hco/9/GRCh38#6564482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30101324-C-A

6564482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30101324-C-T

http://identifiers.org/hco/9/GRCh38#6564483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30101325-C-A

6564483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30101325-C-G

6564621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30101437-T-C

6564627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30101443-C-T

6564647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30101463-T-C

http://identifiers.org/hco/9/GRCh38#6564722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30101532-C-A

6564731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30101541-G-C

6564758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30101567-C-T

6564763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30101582-G-A

6564791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30101608-T-A

6564791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30101608-T-C

6564791-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30101608-T-G

6564942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30101753-C-G

6565033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30101814-G-A

6565045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30101824-G-A

6565207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30101968-G-A

6565207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30101968-G-T

http://identifiers.org/hco/9/GRCh38#6565235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30101996-C-A

6565235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30101996-C-T

6565252-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30102013-T-G

6565276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30102037-G-A

6565276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30102037-G-T

6565315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30102081-G-T

6565322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30102088-G-A

6565322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30102088-G-C

6565322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30102088-G-T

6565327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30102093-G-A

6565327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30102093-G-C

6565327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30102093-G-T

6565331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30102097-G-A

6565331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30102097-G-T

6565387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30102155-G-A

6565387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30102155-G-C

6565404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30102172-G-A

6565411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30102179-A-G

6565429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 30102197-G-A

6565429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 30102197-G-T

6565465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 30102233-T-A

6565471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 30102239-G-C

6565471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 30102239-G-T

6565509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30102278-C-G

6565509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30102278-C-T

6565691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30102384-G-T

6565778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30102482-G-A

6565778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30102482-G-C

6565778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30102482-G-T

6565821-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30102533-T-A

6565821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30102533-T-C

6565855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30102571-T-C

6565855-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30102571-T-G

http://identifiers.org/hco/9/GRCh38#6566616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#30102868-C-A

6566616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30102868-C-T

6566633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30102885-T-C

6566662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30102910-A-G

6568276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30105657-T-C

6568284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30105665-A-G

6568295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30105676-C-G

6568295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30105676-C-T

6568350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30105731-G-C

6568400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30105777-C-G

6568953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30105958-C-T

6568994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30105999-C-G

http://identifiers.org/hco/9/GRCh38#6569037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30106036-A-C

6569037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30106036-A-G

6569038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30106037-G-C

6569052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30106050-C-T

6569090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30106087-A-G

6569098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30106094-G-A

6569126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30106119-G-T

http://identifiers.org/hco/9/GRCh38#6569137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30106130-C-A

6569176-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30106157-A-T

6569263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30106229-G-T

6569316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30106283-C-G

6569316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30106283-C-T

6569375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30106348-C-T

6569384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30106357-T-G

http://identifiers.org/hco/9/GRCh38#6569387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30106360-C-A

6569391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30106364-C-T

6569422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30106394-G-A

6569422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30106394-G-T

6569429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30106401-G-A

http://identifiers.org/hco/9/GRCh38#6569436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30106415-A-C

6569436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30106415-A-G

6575746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30107949-G-A

6575801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30108003-C-T

6575849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30108054-T-C

6575907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30108113-A-G

6575947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30108150-G-C

6575973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30108175-G-C

6586847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30108611-C-T

6586915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30108676-A-G

6586986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30108755-G-A

6586986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30108755-G-C

6587003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30108771-T-C

6587021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30108788-G-A

6587021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30108788-G-T

6587045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30108811-T-A

6587045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30108811-T-C

6587071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30108970-C-G

http://identifiers.org/hco/9/GRCh38#6587076-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30108975-A-C

6587076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30108975-A-T

6587083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30108982-G-T

6587106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30109008-G-A

6587106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30109008-G-C

6587106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30109008-G-T

6587127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30109054-A-G

6587128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30109055-G-A

6587128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30109055-G-T

6587132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30109059-T-C

6587173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30109104-T-C

6587301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30109232-A-G

6587314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30109245-T-C

6587334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30109259-G-A

6587334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30109259-G-T

http://identifiers.org/hco/9/GRCh38#6587335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30109260-C-A

6587335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30109260-C-G

http://identifiers.org/hco/9/GRCh38#6587349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30109274-A-C

6587352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30109277-A-G

6587365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30109301-T-A

6587365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30109301-T-G

http://identifiers.org/hco/9/GRCh38#6587370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30109306-A-C

6587417-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30109358-T-A

6587417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30109358-T-C

6587458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30109391-C-T

6587553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30109481-A-G

6588261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30110752-A-G

6588388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30110867-G-A

6588388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30110867-G-C

6588388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30110867-G-T

http://identifiers.org/hco/9/GRCh38#6588410-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30110889-A-C

6588440-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 30110919-T-A

6588440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 30110919-T-C

6588453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30110932-A-G

6588479-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30110959-A-T

6588512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30110992-T-C

6588531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30111007-T-C

6588531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30111007-T-G

6588533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30111009-G-C

6588543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30111021-G-C

6588545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30111023-G-A

6588545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30111023-G-C

6588545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30111023-G-T

http://identifiers.org/hco/9/GRCh38#6588552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30111030-A-C

6588552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30111030-A-T

6588643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30111120-G-C

6588643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30111120-G-T

http://identifiers.org/hco/9/GRCh38#6588722-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30111199-A-C

6588757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30111227-A-G

6588938-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30111351-A-T

6589012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30111405-C-G

6589061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30111453-G-A

6589082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30111472-G-A

6589082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30111472-G-C

6589082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30111472-G-T

http://identifiers.org/hco/9/GRCh38#6589103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30111494-C-A

6589103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30111494-C-T

6589108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30111499-G-A

6589108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30111499-G-T

6589187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30111582-A-G

http://identifiers.org/hco/9/GRCh38#6590746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#30112660-C-A

6590746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30112660-C-T

6590825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30112731-C-T

http://identifiers.org/hco/9/GRCh38#6590878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#30112770-C-A

6591175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30113354-C-G

6591175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30113354-C-T

6591208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30113386-C-G

http://identifiers.org/hco/9/GRCh38#6591293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30113424-C-A

6591448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30113526-T-C

6591915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30113698-A-G

http://identifiers.org/hco/9/GRCh38#6591944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30113722-C-A

6591944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30113722-C-T

6591971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30113749-G-A

6591971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30113749-G-C

6591990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30113768-A-T

6592003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30113787-G-A

6592003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30113787-G-T

http://identifiers.org/hco/9/GRCh38#6592038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30113823-C-A

6592038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30113823-C-G

6592091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30113854-G-T

6592112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30113875-G-T

6592172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30113933-A-G

6592227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30113988-C-G

6592227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30113988-C-T

6592238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30113999-A-G

6592252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30114013-A-G

6592279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30114040-G-A

6592279-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30114040-G-C

6592279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30114040-G-T

6592300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30114062-G-A

6592300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30114062-G-C

6592300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30114062-G-T

6592302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30114064-G-A

6592302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30114064-G-C

6592302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30114064-G-T

6592310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30114072-T-C

6592352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30114117-T-A

6592352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30114117-T-C

6592352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30114117-T-G

http://identifiers.org/hco/9/GRCh38#6592362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30114127-C-A

6592362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30114127-C-T

http://identifiers.org/hco/9/GRCh38#6592787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30114445-C-A

6592787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30114445-C-G

6592787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30114445-C-T

http://identifiers.org/hco/9/GRCh38#6592994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30114636-C-A

6592994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30114636-C-T

6593006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30114648-G-A

6593006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30114648-G-C

6593006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30114648-G-T

6593057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30114695-C-T

6593288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30114895-A-T

6593500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30115141-C-T

6593504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30115145-G-A

6593528-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30115169-T-A

6594252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30116200-C-G

6594252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30116200-C-T

6594422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30116327-A-G

6594447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30116352-G-C

6594471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30116362-G-A

http://identifiers.org/hco/9/GRCh38#6594752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30116459-C-A

http://identifiers.org/hco/9/GRCh38#6594760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30116467-C-A

6594760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30116467-C-G

6594868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30116564-A-G

6594892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30116588-T-C

6594893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30116589-T-G

6594955-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30116626-T-A

http://identifiers.org/hco/9/GRCh38#6594961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30116632-C-A

http://identifiers.org/hco/9/GRCh38#6594997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30116658-A-C

http://identifiers.org/hco/9/GRCh38#6595108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, stop_gained, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30116769-C-A

6595108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30116769-C-G

6595108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30116769-C-T

6595150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30116817-T-A

6595155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30116822-G-A

6595155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30116822-G-T

6595168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30116835-G-A

6595168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30116835-G-T

6595197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30116863-T-C

6595416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30117031-A-G

6595467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30117081-G-A

6595485-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30117099-T-A

6595488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30117102-G-A

http://identifiers.org/hco/9/GRCh38#6595676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30117277-C-A

6595676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30117277-C-T

6595756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30117351-G-C

6599212-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30119744-A-T

6599231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30119762-G-C

6601974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30120641-C-T

6602010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30120677-C-T

6602043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30120710-A-G

6602044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30120711-T-A

6602045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30120712-G-T

http://identifiers.org/hco/9/GRCh38#6602057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30120724-C-A

6602057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30120724-C-G

6602064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30120731-G-C

6602095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30120746-G-A

6602095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30120746-G-C

6602095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30120746-G-T

http://identifiers.org/hco/9/GRCh38#6602097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30120748-C-A

6602097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30120748-C-T

6602098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30120749-G-A

6602098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30120749-G-T

6602121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30120772-G-A

6602121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30120772-G-T

6602145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30120796-C-G

6602145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30120796-C-T

http://identifiers.org/hco/9/GRCh38#6602175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30120826-A-C

6602242-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30120892-A-T

6602255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30120905-G-A

6602255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30120905-G-T

6602696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30121298-T-C

6602696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30121298-T-G

6602777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30121377-G-C

6604573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30122534-C-T

http://identifiers.org/hco/9/GRCh38#6604628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30122587-A-C

6604713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30122672-G-A

6604868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30122815-G-A

6604868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30122815-G-C

6604885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30122832-T-A

http://identifiers.org/hco/9/GRCh38#6604904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30122849-C-A

6604904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30122849-C-G

6604904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30122849-C-T

http://identifiers.org/hco/9/GRCh38#6604910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30122856-C-A

6604910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30122856-C-G

6604910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30122856-C-T

6604980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30122909-T-C

6604980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30122909-T-G

http://identifiers.org/hco/9/GRCh38#6605017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30122946-C-A

6605017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30122946-C-T

http://identifiers.org/hco/9/GRCh38#6605076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30122966-C-A

6605076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30122966-C-T

http://identifiers.org/hco/9/GRCh38#6605107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30122996-C-A

6605107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30122996-C-G

6605107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30122996-C-T

6605143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30123030-A-G

http://identifiers.org/hco/9/GRCh38#6605161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30123048-C-A

6605161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30123048-C-G

6605161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30123048-C-T

6605313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30123225-T-C

6605325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30123333-G-T

6605431-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30123589-T-G

http://identifiers.org/hco/9/GRCh38#6605501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30123659-C-A

6605501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30123659-C-G

6605501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30123659-C-T

6605647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30123794-T-C

6605751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30123879-T-A

6605758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30123886-C-T

6605834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30123957-A-G

6605873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30123996-G-A

6605873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30123996-G-T

6605888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30124011-T-G

6605961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30124084-T-C

6605962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30124085-T-G

http://identifiers.org/hco/9/GRCh38#6605988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30124108-C-A

http://identifiers.org/hco/9/GRCh38#6606358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30124349-C-A

6606359-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30124350-T-A

6606361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30124352-T-A

6606361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30124352-T-C

http://identifiers.org/hco/9/GRCh38#6606508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30124488-C-A

6606508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30124488-C-T

6606543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30124521-G-C

6606543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30124521-G-T

6606562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30124539-T-C

6606562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30124539-T-G

http://identifiers.org/hco/9/GRCh38#6606644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30124621-C-A

6606644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30124621-C-T

6606687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30124664-C-T

6608838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30125894-A-G

6608961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30126005-G-A

6608961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30126005-G-T

6608996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30126040-C-G

6609003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30126047-G-T

6609147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30126187-G-C

6609152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30126192-G-A

6609152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30126192-G-T

6609209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30126263-C-T

6609227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30126276-C-T

6609293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30126339-T-C

6609320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30126367-C-T

6609414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30126457-G-A

http://identifiers.org/hco/9/GRCh38#6610227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30128857-C-A

6610227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30128857-C-T

6610320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30128950-A-G

6610320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30128950-A-T

6610375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30129005-G-A

6610375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30129005-G-C

6610375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30129005-G-T

6610377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30129007-C-G

6610389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30129016-G-C

6610389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30129016-G-T

6610410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30129040-A-G

6610438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30129068-A-G

6611986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30131374-T-A

6611986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30131374-T-C

6612010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30131354-T-C

http://identifiers.org/hco/9/GRCh38#6612119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30131250-C-A

6612127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30131242-C-G

6612127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30131242-C-T

6612129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30131240-G-A

6612129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30131240-G-C

6612177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30131178-A-G

6616706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30134153-T-C

6616868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30134315-G-A

6616868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30134315-G-C

6617161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30134616-A-G

6617352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30134799-C-G

6617352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30134799-C-T

6617476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30134933-G-A

6617476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30134933-G-C

6617574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30135034-G-T

6617601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30135068-A-G

6617608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30135085-T-C

6617634-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30135119-A-T

6617720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30135205-T-C

6619214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30135384-G-C

6619404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30135553-G-A

6619852-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30135656-A-T

6619917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30135690-G-A

6620049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30135794-G-A

6620049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30135794-G-C

6620049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30135794-G-T

http://identifiers.org/hco/9/GRCh38#6620052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30135801-C-A

6620052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30135801-C-G

6620052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30135801-C-T

6620065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30135817-G-A

6620065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30135817-G-T

6620104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30135856-G-C

6620127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30135879-A-T

6620303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 30136033-A-G

6620328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30136058-G-A

6620328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30136058-G-C

http://identifiers.org/hco/9/GRCh38#6620351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30136085-C-A

6620351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30136085-C-G

6620351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30136085-C-T

http://identifiers.org/hco/9/GRCh38#6620361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30136095-A-C

6620361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30136095-A-G

6620367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30136101-G-A

6620367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30136101-G-T

http://identifiers.org/hco/9/GRCh38#6620374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30136108-A-C

6620374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30136108-A-T

6620379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30136113-C-G

http://identifiers.org/hco/9/GRCh38#6620380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30136114-A-C

6620380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30136114-A-G

6620404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30136122-A-T

http://identifiers.org/hco/9/GRCh38#6620447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30136163-C-A

6620475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30136194-C-T

6620482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30136201-T-A

6620482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30136201-T-C

6620598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30136755-C-G

6620598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30136755-C-T

6620690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30137240-G-A

6620818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30137363-G-C

6623841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30137520-A-G

6623938-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30137614-A-T

6624076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30137772-C-T

6624187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30137868-A-G

6624377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30138498-G-A

6624427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30138546-A-G

6624468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30138588-G-C

6624589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30138703-T-G

6624685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30138774-A-T

6624699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30138788-C-T

6624847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30138873-G-A

6624898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30138905-G-A

6625271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30139239-C-G

http://identifiers.org/hco/9/GRCh38#6625357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30139318-A-C

6625357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30139318-A-G

6627888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30139913-C-T

6627900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30139925-T-C

http://identifiers.org/hco/9/GRCh38#6627929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30139948-A-C

6628468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30140052-C-G

6628856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30140354-C-G

6628955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30140455-G-A

6628994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30140494-C-G

http://identifiers.org/hco/9/GRCh38#6628995-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#30140495-A-C

6628995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30140495-A-G

6629085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30140576-T-C

6629359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30140772-C-T

6629401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30140794-G-C

6629683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30140997-C-G

6629710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30141024-G-A

6629887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30141204-T-C

6629905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30141219-T-G

6629998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30141290-C-T

6630007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30141299-T-C

6630378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30141707-G-C

6630478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30141769-G-C

6630479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30141770-C-T

6630481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30141772-T-C

6630658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30141950-A-G

6630836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30142117-G-C

http://identifiers.org/hco/9/GRCh38#6630980-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#30142262-A-C

6631213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30142665-G-C

6631240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30142694-C-T

http://identifiers.org/hco/9/GRCh38#6631302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30142887-C-A

6631332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30142964-G-C

6631360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30142995-C-T

6631437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30143058-G-A

6631437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30143058-G-C

6631641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30143254-G-C

6631641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30143254-G-T

6632115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30143443-A-G

6632121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30143452-T-C

6632156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30143479-G-A

6632750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30144386-G-C

6632788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30144427-A-G

6632839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30144501-G-T

6633035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30144616-G-T

6633052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30144633-A-G

6633236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30144802-C-T

6633281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30144836-A-G

6634726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30144950-G-A

6634726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30144950-G-T

6634797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30145018-G-C

http://identifiers.org/hco/9/GRCh38#6634841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30145060-C-A

6634857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30145076-C-T

http://identifiers.org/hco/9/GRCh38#6635087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30145246-C-A

6635087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30145246-C-T

6635178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30145316-C-G

http://identifiers.org/hco/9/GRCh38#6635188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30145337-C-A

6635241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30145447-C-G

6635269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30145533-G-C

6635269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30145533-G-T

6635429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30145694-A-T

6635489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30145749-C-T

6640009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30147423-C-G

6640052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30147483-C-G

6640062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30147494-C-G

6640062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30147494-C-T

6640090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30147523-C-T

6640109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30147543-T-C

6640162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30147604-G-C

6640173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30147615-C-G

6640175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30147617-C-T

6640292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30147711-G-C

6640478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30147844-C-T

6640608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30147996-T-C

6640610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30147998-G-A

6640630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30148018-G-A

6640631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30148019-G-A

6640631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30148019-G-T

6640808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30148200-G-C

6641187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30148605-T-C

6641346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30148760-G-A

6641437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30148825-G-A

6641437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30148825-G-T

http://identifiers.org/hco/9/GRCh38#6641449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30148837-C-A

http://identifiers.org/hco/9/GRCh38#6641450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30148838-C-A

6641507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30148884-A-T

6641641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30149167-G-A

6641641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30149167-G-T

6641653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30149179-T-C

6641664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30149189-T-C

6641811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30149331-A-G

6641852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30149355-T-C

6641936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30149420-G-A

6642047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30149517-T-G

6642050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30149520-T-A

6642088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30149558-C-T

http://identifiers.org/hco/9/GRCh38#6642182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30149642-A-C

http://identifiers.org/hco/9/GRCh38#6642201-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30149657-A-C

6642332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30149788-C-G

6642346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30149802-A-G

http://identifiers.org/hco/9/GRCh38#6642543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30149900-A-C

6642706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30149941-T-C

6642755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30149985-C-G

6642826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30150051-C-T

6642924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30150180-G-T

6642937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30150193-T-C

6643043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30150288-G-A

6643046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30150291-C-T

6643056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30150301-C-G

6643058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30150303-C-T

6643296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30150662-G-A

6643296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30150662-G-C

6643300-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30150666-A-T

6643362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30150735-A-T

6643414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30150788-T-C

http://identifiers.org/hco/9/GRCh38#6643525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#30150881-C-A

6643525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30150881-C-T

6643529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30150885-A-G

6643542-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30150908-T-A

6643547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30150929-G-A

6643547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30150929-G-C

6643617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30151017-C-G

6643646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30151047-A-T

6643692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

http://identifiers.org/hco/9/GRCh38#6644047-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30151312-A-C

6644063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30151328-G-A

6644063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30151328-G-C

6644063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30151328-G-T

6644129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30151385-T-C

6644136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30151392-G-A

6644136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30151392-G-T

6644249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30151506-T-C

6644268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30151525-G-A

6644268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30151525-G-T

6644282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30151538-C-T

6644299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30151555-G-A

6644365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30151637-C-G

6644368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30151640-G-C

http://identifiers.org/hco/9/GRCh38#6644397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30151681-C-A

6644397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30151681-C-T

6644432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30151696-C-G

6644432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30151696-C-T

http://identifiers.org/hco/9/GRCh38#6644435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30151699-C-A

6644435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30151699-C-T

6644466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30151723-G-A

6644466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30151723-G-T

http://identifiers.org/hco/9/GRCh38#6644512-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30151738-A-C

6644555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30151775-C-G

6644555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30151775-C-T

6644583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30151793-T-A

6644583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30151793-T-C

6644591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30151801-A-G

6644591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30151801-A-T

6644654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30151864-G-A

6644654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30151864-G-T

6644681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30151891-T-C

6644711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30151939-G-A

6644711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30151939-G-T

6644721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30151949-G-A

6644721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30151949-G-C

6644721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30151949-G-T

http://identifiers.org/hco/9/GRCh38#6644768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30151989-C-A

6644768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30151989-C-T

6644802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30152024-G-C

6644802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30152024-G-T

http://identifiers.org/hco/9/GRCh38#6645012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30152218-A-C

http://identifiers.org/hco/9/GRCh38#6645126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#30152315-C-A

6645126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, undefined
orthologous variants: 30152315-C-G

6645175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron variant
orthologous variants: 30152340-G-A

6645175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron variant
orthologous variants: 30152340-G-C

6645175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron variant
orthologous variants: 30152340-G-T

http://identifiers.org/hco/9/GRCh38#6645196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#30152361-C-A

6645196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, undefined
orthologous variants: 30152361-C-T

6645198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, undefined
orthologous variants: 30152363-G-A

6645198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, undefined
orthologous variants: 30152363-G-C

6645198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: intron_variant, undefined
orthologous variants: 30152363-G-T

6645290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: synonymous variant
orthologous variants: 30152436-A-G

http://identifiers.org/hco/9/GRCh38#6645361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30152507-C-A

6645361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: missense variant
orthologous variants: 30152507-C-G

6645361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: missense variant
orthologous variants: 30152507-C-T

6645377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: synonymous variant
orthologous variants: 30152538-G-A

6645377-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: synonymous variant
orthologous variants: 30152538-G-C

6645377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: synonymous variant
orthologous variants: 30152538-G-T

http://identifiers.org/hco/9/GRCh38#6645382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30152543-C-A

6645382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: missense variant
orthologous variants: 30152543-C-T

http://identifiers.org/hco/9/GRCh38#6645401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30152562-C-A

6645401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: synonymous variant
orthologous variants: 30152562-C-G

6645401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: synonymous variant
orthologous variants: 30152562-C-T

6645405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: missense variant
orthologous variants: 30152566-G-A

6645405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: missense variant
orthologous variants: 30152566-G-T

6645504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5 prime UTR variant
orthologous variants: 30152665-G-A

6645504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5 prime UTR variant
orthologous variants: 30152665-G-C

6645504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5 prime UTR variant
orthologous variants: 30152665-G-T

http://identifiers.org/hco/9/GRCh38#6645527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30152681-C-A

6645527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5 prime UTR variant
orthologous variants: 30152681-C-T

6645587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5 prime UTR variant
orthologous variants: 30152743-T-A

6645587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5 prime UTR variant
orthologous variants: 30152743-T-C

6645587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5 prime UTR variant
orthologous variants: 30152743-T-G

http://identifiers.org/hco/9/GRCh38#6645604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30152758-C-A

6645604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5 prime UTR variant
orthologous variants: 30152758-C-G

6645604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5 prime UTR variant
orthologous variants: 30152758-C-T

6645663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5 prime UTR variant
orthologous variants: 30152790-G-A

6645663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5 prime UTR variant
orthologous variants: 30152790-G-T

http://identifiers.org/hco/9/GRCh38#6645667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#30152794-C-A

6645667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4313
most severe consequence: 5 prime UTR variant
orthologous variants: 30152794-C-T