6310362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5 prime UTR variant
orthologous variants: 125357843-G-A

6310362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5 prime UTR variant
orthologous variants: 125357843-G-T

http://identifiers.org/hco/12/GRCh38#6310372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125357833-C-A

6310376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, splice_donor_variant
orthologous variants: 125357829-T-C

http://identifiers.org/hco/12/GRCh38#6310395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125357802-C-A

6310395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 125357802-C-T

6310442-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 125357755-T-A

6310442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 125357755-T-C

6310538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, undefined
orthologous variants: 125357631-A-G

http://identifiers.org/hco/12/GRCh38#6310609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125357588-C-A

6310738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125357419-G-A

6310738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125357419-G-T

http://identifiers.org/hco/12/GRCh38#6310791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#125357368-C-A

6310791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 125357368-C-T

6310808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125357350-G-A

6310829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125357330-G-T

http://identifiers.org/hco/12/GRCh38#6310929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125357199-A-C

6310929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125357199-A-G

6310960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125357168-A-G

6310988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125357148-T-C

6310998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125357138-G-A

6310998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125357138-G-T

6311009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125357127-G-A

6311031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125357105-G-A

6311031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125357105-G-T

6311132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125357002-G-A

6311132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125357002-G-T

6311206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125356931-C-T

http://identifiers.org/hco/12/GRCh38#6311231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125356904-C-A

6311383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125356757-C-T

6311537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125356595-G-A

http://identifiers.org/hco/12/GRCh38#6311745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125356283-C-A

6311772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125356209-C-T

6311775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125356206-A-G

6312014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125355988-G-A

6312014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125355988-G-T

6312015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125355987-T-C

6312042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125355972-G-A

6312042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125355972-G-T

6312197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125355830-G-A

6312197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125355830-G-T

6312414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125355613-A-G

6312421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125355606-G-A

6312421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125355606-G-C

6312421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125355606-G-T

6312435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125355594-T-C

6312435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125355594-T-G

6312436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125355593-G-A

6312437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125355592-T-A

6312437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125355592-T-C

http://identifiers.org/hco/12/GRCh38#6312440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125355589-C-A

6312440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125355589-C-T

http://identifiers.org/hco/12/GRCh38#6312473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125355560-C-A

6312473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125355560-C-T

6312687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125355384-C-T

6312852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125355237-G-A

6312983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125355111-A-G

6313034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125355060-G-A

6313034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125355060-G-T

6313124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125354978-A-G

6313226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125354877-T-C

6313259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125354850-G-T

6313291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125354819-T-C

6313293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125354817-G-A

6313293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125354817-G-C

6313293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125354817-G-T

6313318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125354781-G-A

6313318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125354781-G-T

6313362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125354736-C-T

6313472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125354624-G-A

6313576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125354541-G-T

6313622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 125354505-C-T

6313686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125354441-G-A

6313686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125354441-G-T

http://identifiers.org/hco/12/GRCh38#6313773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125354354-C-A

6313773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125354354-C-T

6313788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125354339-A-G

6313788-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125354339-A-T

6313859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125354263-T-C

6313859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125354263-T-G

6313877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125354247-A-G

6313922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125354187-G-T

6313923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125354186-G-A

6313923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125354186-G-T

6314126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125353838-C-G

6314229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125353698-G-A

6314229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125353698-G-T

6314845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352977-A-G

6314853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352969-A-G

http://identifiers.org/hco/12/GRCh38#6314854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125352968-C-A

6314854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352968-C-G

6314854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352968-C-T

6314877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352958-T-C

http://identifiers.org/hco/12/GRCh38#6314903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125352945-C-A

6314903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352945-C-T

6314920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352936-A-G

http://identifiers.org/hco/12/GRCh38#6314925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125352931-C-A

6314925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352931-C-T

http://identifiers.org/hco/12/GRCh38#6314926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125352930-A-C

6314926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352930-A-G

http://identifiers.org/hco/12/GRCh38#6314949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125352907-C-A

6314999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 125352855-C-T

6315248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352555-G-T

http://identifiers.org/hco/12/GRCh38#6315249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125352554-C-A

http://identifiers.org/hco/12/GRCh38#6315257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125352546-A-C

http://identifiers.org/hco/12/GRCh38#6315265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125352541-C-A

6315265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352541-C-T

http://identifiers.org/hco/12/GRCh38#6315278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125352525-C-A

6315352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352461-A-G

6315369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352445-G-T

6315419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352418-G-A

6315419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352418-G-T

6315468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352377-T-C

6315473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352372-T-C

6315497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352351-G-A

6315535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352316-A-G

http://identifiers.org/hco/12/GRCh38#6315700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125352151-C-A

6315742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352111-G-A

6315742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352111-G-C

6315742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352111-G-T

6315745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352108-A-G

6315770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352077-A-G

6315771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352076-G-A

6315771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352076-G-T

6315798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352055-G-A

6315798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352055-G-T

6315816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352040-A-G

6315829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352026-G-A

6315829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352026-G-T

http://identifiers.org/hco/12/GRCh38#6315830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125352025-C-A

6315830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352025-C-T

6315834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352022-G-A

6315834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125352022-G-T

6315934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125351920-A-G

http://identifiers.org/hco/12/GRCh38#6315987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125351894-C-A

6315987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125351894-C-T

http://identifiers.org/hco/12/GRCh38#6315994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125351887-C-A

6316057-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125351821-T-A

6316057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125351821-T-C

6316076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125351802-G-A

6316134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125351718-A-G

6316134-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125351718-A-T

6316155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125351712-G-A

6316155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125351712-G-C

6316155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125351712-G-T

6316187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125351688-T-C

6316226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125351668-G-A

6316226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125351668-G-T

6316258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125351636-T-C

6316261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125351633-G-A

6316261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125351633-G-T

http://identifiers.org/hco/12/GRCh38#6316305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125351589-C-A

6316305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125351589-C-G

6316305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125351589-C-T

6316354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125351540-G-A

6316354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125351540-G-T

http://identifiers.org/hco/12/GRCh38#6316551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125351392-C-A

6316551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125351392-C-T

6316997-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125350466-T-G

6317100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125350367-T-G

6317227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125350241-G-A

6317227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125350241-G-T

http://identifiers.org/hco/12/GRCh38#6317245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125350224-C-A

6317245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125350224-C-T

6317290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125350191-T-C

http://identifiers.org/hco/12/GRCh38#6317291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125350190-C-A

http://identifiers.org/hco/12/GRCh38#6317310-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125350171-A-C

6317310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125350171-A-G

6317426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125350052-G-A

6317426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125350052-G-T

http://identifiers.org/hco/12/GRCh38#6317531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125349938-C-A

6317531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 125349938-C-T

http://identifiers.org/hco/12/GRCh38#6317661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125349809-C-A

6317812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125349618-G-A

6317812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125349618-G-T

6317857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 125349576-A-G

6317977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125349456-A-G

6317977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125349456-A-T

6318011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125349431-A-G

6318011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125349431-A-T

6318029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125349413-A-G

6318071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125349364-G-T

http://identifiers.org/hco/12/GRCh38#6318094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125349347-C-A

6318099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125349338-G-A

6318099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125349338-G-T

6318161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125349279-A-G

6318211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125349236-G-T

6318237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125349211-C-T

6318338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125349101-C-T

6318446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125348993-G-A

6318447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125348992-G-A

6318461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125348978-T-C

6318469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125348975-G-A

6318538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125347877-C-G

6318539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125347876-C-G

6318539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125347876-C-T

6318565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125347850-G-A

6318565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125347850-G-T

6318596-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125347819-T-A

http://identifiers.org/hco/12/GRCh38#6318608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125347807-C-A

6318608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125347807-C-T

6318653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125347762-T-C

6318688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125347732-A-G

6318728-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125347692-T-G

6318760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125347660-T-C

6318881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 125347539-C-T

6318937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 125347515-G-A

6319131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125347318-G-A

6319132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125347317-A-G

http://identifiers.org/hco/12/GRCh38#6319135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125347314-C-A

6319135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125347314-C-T

6319138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125347311-G-A

6319138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125347311-G-C

6319138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125347311-G-T

6319153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125347296-G-T

6323159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125345260-C-T

http://identifiers.org/hco/12/GRCh38#6323500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#125344978-A-C

6323717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125344797-C-T

6323799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125344702-C-T

6324270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125344289-T-C

6324302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125344259-G-A

6324302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125344259-G-C

6324536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125344022-C-T

http://identifiers.org/hco/12/GRCh38#6324544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125344014-A-C

http://identifiers.org/hco/12/GRCh38#6324853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125343738-A-C

6324853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125343738-A-G

6325592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125342141-G-A

http://identifiers.org/hco/12/GRCh38#6325622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125342131-C-A

http://identifiers.org/hco/12/GRCh38#6325687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125342068-C-A

6325699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125342049-A-G

6325755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125341998-G-C

6325775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125341978-C-G

6326406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125341716-T-C

http://identifiers.org/hco/12/GRCh38#6326505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125341619-C-A

6326524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 125341600-A-G

http://identifiers.org/hco/12/GRCh38#6326604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#125341529-C-A

6326604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125341529-C-G

6326604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125341529-C-T

6326616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125341516-G-A

6326616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125341516-G-T

6326665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125341483-T-A

6326700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125341439-G-A

6326700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125341439-G-T

6326752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125341358-G-C

6326761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125341351-G-A

http://identifiers.org/hco/12/GRCh38#6327074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125341049-C-A

6327074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125341049-C-T

6327111-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125340820-T-A

6327111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125340820-T-G

6327155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125340778-A-G

6327193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125340744-G-A

6327193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125340744-G-T

6327238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125340696-T-C

6327314-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125340623-T-A

http://identifiers.org/hco/12/GRCh38#6327352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125340585-A-C

6327471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125340466-C-G

6327615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125340322-G-A

6327615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125340322-G-T

6327662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125340275-G-A

6327662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125340275-G-T

6327927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125340022-G-A

6327927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125340022-G-T

http://identifiers.org/hco/12/GRCh38#6327981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125339978-C-A

6327981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125339978-C-G

6327981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125339978-C-T

6327986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125339973-G-A

6327986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125339973-G-C

6327986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125339973-G-T

6328010-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125339954-T-A

6328010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125339954-T-C

6328010-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125339954-T-G

http://identifiers.org/hco/12/GRCh38#6328124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#125339840-C-A

6328159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125339805-C-T

6328297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125339680-G-A

6328297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125339680-G-T

6328348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25562
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125339628-A-G