71808491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110505869-A-G

71808542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110505816-G-A

71808775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110505580-T-A

http://identifiers.org/hco/16/GRCh38#71808989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110505364-C-A

71808989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110505364-C-T

http://identifiers.org/hco/16/GRCh38#71809025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110505328-C-A

71809025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110505328-C-G

71809025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110505328-C-T

71809249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110505141-G-A

71809249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110505141-G-C

71809249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110505141-G-T

71809251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110505139-G-A

71809310-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110505079-T-A

71809316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110505073-A-G

71809543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110504833-A-G

71809557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110504820-A-G

http://identifiers.org/hco/16/GRCh38#71809733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110504652-C-A

71809735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110504650-A-G

71810276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110504417-A-G

71811419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110503986-G-C

71811505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110503901-G-A

71816661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110500106-G-A

71816849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110499950-C-G

71816849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110499950-C-T

71816981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110499818-A-G

71817100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110499693-T-C

http://identifiers.org/hco/16/GRCh38#71817488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110499392-C-A

71817499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110499381-A-G

71817499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110499381-A-T

71817873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110499235-C-G

71818104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 110499061-T-C

71818777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron variant
orthologous variants: 110497851-G-A

71821066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron variant
orthologous variants: -T-A

71821066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron variant
orthologous variants: -T-C

71821074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron variant
orthologous variants: -T-A

71821074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron variant
orthologous variants: -T-C

71821078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron variant
orthologous variants: -T-A

71821082-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron variant
orthologous variants: -T-A

71830659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron variant
orthologous variants: 110485591-A-G

71831768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron variant
orthologous variants: 110485209-C-G

71833529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron variant
orthologous variants: 110484414-C-T

http://identifiers.org/hco/16/GRCh38#71833546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110484397-C-A

71833546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron variant
orthologous variants: 110484397-C-G

71834331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110483731-A-G

http://identifiers.org/hco/16/GRCh38#71834421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110483648-C-A

71834421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110483648-C-G

71834421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110483648-C-T

71834452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110483614-T-C

71834452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110483614-T-G

71834499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110483567-T-A

71834499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110483567-T-C

71834550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110483526-G-A

71838376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron variant
orthologous variants: 110479278-C-G

71838424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron variant
orthologous variants: 110479230-G-C

71838904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron variant
orthologous variants: 110479097-G-T

71838958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron variant
orthologous variants: 110479043-T-C

71838976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron variant
orthologous variants: 110479022-G-C

http://identifiers.org/hco/16/GRCh38#71840200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110477086-A-C

71840207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron variant
orthologous variants: 110477079-C-T

71840443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron variant
orthologous variants: 110476143-C-T

71840957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron variant
orthologous variants: 110475093-C-T

71842368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron variant
orthologous variants: 110474929-A-G

http://identifiers.org/hco/16/GRCh38#71842382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110474910-C-A

71842561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron variant
orthologous variants: 110474747-T-C

71845213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron variant
orthologous variants: 110464787-C-T

71845606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron variant
orthologous variants: 110464574-C-T

71845866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron variant
orthologous variants: 110464502-G-A

71845866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron variant
orthologous variants: 110464502-G-C

71845895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron variant
orthologous variants: 110464473-C-T

http://identifiers.org/hco/16/GRCh38#71845980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110464389-C-A

71845980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110464389-C-G

71845980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110464389-C-T

71846081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110464284-T-C

71846081-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110464284-T-G

71846380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110463969-C-G

71846636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110463721-A-G

71846746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110463604-C-T

71847350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110462816-A-G

71847645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110462522-T-C

71847735-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110462436-T-A

71847745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110462426-G-A

71847767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110462402-A-G

http://identifiers.org/hco/16/GRCh38#71847862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110462144-C-A

71847862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110462144-C-T

71848187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110461846-G-C

71848356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110461174-G-T

71849439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110460546-G-A

71849484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110460501-G-A

71849484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110460501-G-T

71849499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110460491-T-C

http://identifiers.org/hco/16/GRCh38#71849636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110460360-C-A

71849636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110460360-C-T

71849661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110460335-G-A

71849661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110460335-G-T

71849699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110460297-C-T

71850348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 110459651-C-G

71850356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 110459643-T-A

71850413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 110459586-G-A

71850413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 110459586-G-C

71850654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 110459351-G-A

71850654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 110459351-G-C

71851116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 110458889-C-G

71851116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 110458889-C-T

71851223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 110458782-C-T

71851705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110458300-A-G

71851736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 110458269-G-A

71851736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 110458269-G-T

71851737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 110458268-C-G

71851737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 110458268-C-T

71851852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110458152-T-G

71851868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110458141-A-G

71851938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110458074-A-G

71851938-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110458074-A-T

71852204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110457809-G-T

71852387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110457612-T-C

http://identifiers.org/hco/16/GRCh38#71852476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110457526-C-A

71852476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110457526-C-G

71852476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110457526-C-T

71852494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110457495-T-C

71852534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110457455-T-A

71852555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110457436-A-G

71852601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110457393-G-A

71852685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110457322-T-C

71852685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110457322-T-G

http://identifiers.org/hco/16/GRCh38#71853107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110456958-C-A

71853123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110456946-A-G

http://identifiers.org/hco/16/GRCh38#71853307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110456781-C-A

71853307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110456781-C-T

71853323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110456765-G-T

71853662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110456433-G-T

http://identifiers.org/hco/16/GRCh38#71853885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110456210-C-A

71853885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110456210-C-T

71854498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110455656-G-C

71854498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110455656-G-T

http://identifiers.org/hco/16/GRCh38#71854688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110455555-C-A

71854688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110455555-C-G

71854907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110455392-G-T

71854988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110455315-C-T

71855039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110455261-G-A

71855039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110455261-G-T

http://identifiers.org/hco/16/GRCh38#71855084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110455216-C-A

71855084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110455216-C-T

http://identifiers.org/hco/16/GRCh38#71855106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110455196-C-A

71855106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110455196-C-T

71855233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110455072-T-C

71855506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110454855-G-A

71855673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110454707-G-T

http://identifiers.org/hco/16/GRCh38#71856005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110454393-C-A

71856005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110454393-C-T

71856669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110453746-T-C

71856710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110453705-G-A

71856710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110453705-G-T

71856789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110453627-A-G

71856814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110453602-G-T

71857532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110452918-C-T

71857614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110452834-A-G

71857807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110452683-T-G

71859051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110451789-C-G

71859054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110451786-T-C

71859068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110451772-T-C

71859084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110451756-A-T

http://identifiers.org/hco/16/GRCh38#71859537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110451700-C-A

71859539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110451698-C-G

http://identifiers.org/hco/16/GRCh38#71859591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110451646-A-C

71859591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110451646-A-G

71859591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110451646-A-T

71859605-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110451636-T-A

71859605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110451636-T-C

71859605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110451636-T-G

71859654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110451587-T-G

71859672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110451570-A-G

71859768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110451475-G-A

71859780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110451463-G-A

71859780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110451463-G-T

71859810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110451433-T-A

71859810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110451433-T-C

http://identifiers.org/hco/16/GRCh38#71859835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110451407-C-A

71859835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110451407-C-T

71860028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110451238-G-T

71860091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110451175-C-T

71860132-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 110451134-T-A

71860164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110451102-C-T

71860587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110450679-C-G

71860684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110450582-A-G

71860716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110450550-A-G

http://identifiers.org/hco/16/GRCh38#71860808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110450479-C-A

71860808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110450479-C-T

71861298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110450324-G-A

71861398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110450051-C-G

71861457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110449994-G-A

71861459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110449992-T-C

71861579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110449878-A-G

http://identifiers.org/hco/16/GRCh38#71861638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110449816-C-A

71861638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110449816-C-T

71861701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110449756-C-T

71861709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110449748-C-T

71861726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110449730-C-G

71861788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 110449671-G-A

71861809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 110449650-C-T

71861875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 110449584-G-A

71861890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 110449569-C-T

71864288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110448337-T-C

71864288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110448337-T-G

71864294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110448331-C-G

71864388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110448279-A-G

71864410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110448237-T-C

71864430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110448217-A-G

71864580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110448111-G-C

http://identifiers.org/hco/16/GRCh38#71864607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110448105-C-A

71864607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110448105-C-G

71864607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110448105-C-T

71864870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110448001-C-G

71865241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110447630-C-T

71865395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110447341-T-C

71865997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110446561-G-A

71866063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110446497-A-G

71866259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110446168-A-G

71866341-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110446072-T-A

71866749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110445719-G-A

71867001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110445057-A-G

71867063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110444999-A-G

71867250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110444810-A-G

71867257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110444803-A-G

71867552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110444705-G-A

71867584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110444686-G-T

71867644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110444667-C-T

71867831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110444595-A-G

71868486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110443980-C-T

71869002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110443704-G-A

71870843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110441243-T-G

71870865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110441221-G-A

71870929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110441181-G-A

71871209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110440711-C-G

71871209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110440711-C-T

71871681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110439810-A-T

71873030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110439125-G-A

71875963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110438549-G-A

71875995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110438517-T-A

71875995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110438517-T-C

71878442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110437801-T-C

71879399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110436577-C-G

71879424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110436553-T-C

71879424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110436553-T-G

71879535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110436451-C-T

71879589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110436401-T-C

71879694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110436306-C-T

71879843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110436210-A-G

71879930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110436134-T-C

71879958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 110436106-G-A

71880006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 110436058-T-C

71880061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110435984-T-C

71880167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110435883-G-A

71880167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110435883-G-C

71880167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110435883-G-T

http://identifiers.org/hco/16/GRCh38#71880178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110435872-A-C

http://identifiers.org/hco/16/GRCh38#71880201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110435849-C-A

71880326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110435735-T-A

http://identifiers.org/hco/16/GRCh38#71880342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110435719-A-C

71880342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110435719-A-G

71880408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110435656-A-G

71880420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110435639-C-T

71880495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110435563-G-A

71880799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110435352-A-G

71880849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110435308-G-A

71880881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110435276-C-T

71880882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110435275-A-G

71880901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110435259-T-C

71880907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110435253-G-A

71880917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110435243-C-T

71881000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110435161-T-C

http://identifiers.org/hco/16/GRCh38#71881082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110434979-A-C

71881239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110434850-A-G

71881274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110434817-T-C

http://identifiers.org/hco/16/GRCh38#71882414-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110433860-A-C

71882618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110433658-G-A

71882825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110433450-T-C

71882969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110433312-G-T

71882975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110433300-G-C

71883054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110433215-A-G

71883067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110433201-C-G

71883067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110433201-C-T

71883137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110433128-G-T

71883330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110432933-G-A

71883340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110432923-G-A

71883350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110432913-G-A

71883350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110432913-G-T

71883445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110432825-C-G

71883445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110432825-C-T

http://identifiers.org/hco/16/GRCh38#71883475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110432795-C-A

71883523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110432741-A-G

http://identifiers.org/hco/16/GRCh38#71883797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110432514-C-A

71883797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110432514-C-T

71884014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110432398-G-A

71884125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110432291-A-G

http://identifiers.org/hco/16/GRCh38#71884171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110432239-C-A

71884171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110432239-C-T

71884172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110432238-G-A

71884172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110432238-G-C

71884172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110432238-G-T

http://identifiers.org/hco/16/GRCh38#71884362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110432051-C-A

71884401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110432015-G-C

71884504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110431918-G-T

http://identifiers.org/hco/16/GRCh38#71884528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110431894-C-A

71884528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110431894-C-T

http://identifiers.org/hco/16/GRCh38#71884555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110431867-C-A

71884555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110431867-C-T

71884565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110431858-T-C

71884577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110431843-C-G

http://identifiers.org/hco/16/GRCh38#71884620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110431800-C-A

71884620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110431800-C-T

71884653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110431767-G-T

71884717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110431690-A-G

http://identifiers.org/hco/16/GRCh38#71885166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110431638-C-A

71885166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110431638-C-T

http://identifiers.org/hco/16/GRCh38#71885205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110431599-C-A

http://identifiers.org/hco/16/GRCh38#71885261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110431546-C-A

71885261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33279
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110431546-C-T