194641881-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30380308-T-G

http://identifiers.org/hco/3/GRCh38#194641901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30380327-C-A

194641901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30380327-C-G

194641901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30380327-C-T

194641932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30380354-T-C

194641932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30380354-T-G

194642007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30380436-A-G

http://identifiers.org/hco/3/GRCh38#194642010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30380441-C-A

194642010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30380441-C-T

194642038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30380469-T-A

194642038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30380469-T-C

194642038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30380469-T-G

194642043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30380474-A-G

194642063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30380497-C-T

194642221-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 30380654-T-A

194642306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30380732-G-A

194642306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30380732-G-T

http://identifiers.org/hco/3/GRCh38#194642398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30380834-C-A

194642398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30380834-C-T

http://identifiers.org/hco/3/GRCh38#194642401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30380837-C-A

194642401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30380837-C-G

194642490-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30380913-T-G

194644735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30383626-C-T

194644758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30383649-A-G

194646060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30384156-G-T

194646238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 30384322-G-A

194646545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30384532-G-T

194646700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30384671-T-C

194646773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30384702-G-A

194646853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30384751-C-T

194648942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30386758-G-C

194648942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30386758-G-T

194650824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30387868-A-G

194650962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30388004-A-G

194651098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30388130-A-G

http://identifiers.org/hco/3/GRCh38#194651320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30388306-C-A

194651444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30388403-T-C

http://identifiers.org/hco/3/GRCh38#194651474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30388426-C-A

194651474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30388426-C-T

194651531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30388473-G-C

http://identifiers.org/hco/3/GRCh38#194651563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30388506-C-A

194651564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30388507-T-C

194651661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30388588-G-A

194651661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30388588-G-C

194651661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30388588-G-T

194651675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30388594-T-C

194652037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30389358-A-G

194652039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30389359-G-A

194652159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30389478-T-C

194652177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30389495-T-C

194652296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30389577-T-C

194652329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30389606-G-T

194652453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30389724-T-C

194652516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30389785-G-C

194652704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30389966-A-G

194652807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30390061-G-A

194652848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: missense variant
orthologous variants: 30390102-G-A

http://identifiers.org/hco/3/GRCh38#194652984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30390220-C-A

194652984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: synonymous variant
orthologous variants: 30390220-C-T

194653022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: missense variant
orthologous variants: 30390258-G-A

194653028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: missense variant
orthologous variants: 30390264-G-A

http://identifiers.org/hco/3/GRCh38#194653067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30390279-A-C

194653067-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: missense variant
orthologous variants: 30390279-A-T

194653104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: synonymous variant
orthologous variants: 30390316-G-A

194653104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: synonymous variant
orthologous variants: 30390316-G-C

194653105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: missense variant
orthologous variants: 30390317-G-A

194653188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron variant
orthologous variants: 30390407-C-T

194657693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron variant
orthologous variants: 30391015-C-G

194657695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron variant
orthologous variants: 30391016-C-T

194657719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron variant
orthologous variants: 30391039-G-T

http://identifiers.org/hco/3/GRCh38#194657750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30391070-C-A

http://identifiers.org/hco/3/GRCh38#194657832-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30391155-A-C

194657935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron variant
orthologous variants: 30391316-G-A

194658672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron variant
orthologous variants: 30391726-T-C

http://identifiers.org/hco/3/GRCh38#194658828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30391885-C-A

194658828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron variant
orthologous variants: 30391885-C-T

194658852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron variant
orthologous variants: 30391905-T-A

194658860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron variant
orthologous variants: 30391913-G-A

194658860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron variant
orthologous variants: 30391913-G-C

194658860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron variant
orthologous variants: 30391913-G-T

194658894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron variant
orthologous variants: 30391948-G-A

194658894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron variant
orthologous variants: 30391948-G-C

194658894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: intron variant
orthologous variants: 30391948-G-T

194659142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30392195-G-A

194659142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30392195-G-T

194659221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30392263-T-C

194659221-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30392263-T-G

http://identifiers.org/hco/3/GRCh38#194659231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30392273-A-C

194659231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30392273-A-G

http://identifiers.org/hco/3/GRCh38#194659239-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30392281-A-C

194659239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30392281-A-G

194659239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30392281-A-T

194659556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30392914-C-G

194659917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30393232-T-C

194659946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30393261-G-A

194659949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30393264-G-A

194659949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30393264-G-C

194659949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30393264-G-T

http://identifiers.org/hco/3/GRCh38#194659966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30393286-C-A

194659966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30393286-C-T

194659967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30393287-G-A

194660097-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 30393388-T-G

http://identifiers.org/hco/3/GRCh38#194660274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30394087-C-A

194660274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30394087-C-T

194660281-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30394094-T-A

http://identifiers.org/hco/3/GRCh38#194660321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30394113-C-A

194660346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30394131-C-T

194660434-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30394210-T-A

194660575-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30394338-T-A

http://identifiers.org/hco/3/GRCh38#194660612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30394365-C-A

194660612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30394365-C-T

http://identifiers.org/hco/3/GRCh38#194660688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30394618-C-A

http://identifiers.org/hco/3/GRCh38#194660779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30394695-C-A

194660779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 30394695-C-T

194660793-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 30394706-T-G

194660894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 30394799-G-A

194660997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30394904-A-G

194661436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30395249-C-T

194661525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30395307-C-T

194661554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30395319-C-T

194661930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30395887-A-G

194662061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30396028-C-T

194662164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30396080-T-A

194662191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30396102-G-A

194662191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30396102-G-T

http://identifiers.org/hco/3/GRCh38#194665448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30399666-C-A

http://identifiers.org/hco/3/GRCh38#194665463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30399681-C-A

194665463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30399681-C-G

194665546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30399766-T-C

194665549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 30399769-T-A

194665982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30400523-C-T

194666085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30400758-T-C

http://identifiers.org/hco/3/GRCh38#194666090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30400763-C-A

194666151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30400828-T-C

194666151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30400828-T-G

194666152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30400829-A-G

194666152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30400829-A-T

194666173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30400849-G-T

194666308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30400979-G-A

194666413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30401092-C-T

194666532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 30401429-A-G

194669149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30402396-A-T

194669205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30402441-C-T

194669238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30402474-C-T

194669373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30402613-A-G

194669965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30404327-G-A

194669965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30404327-G-T

194669978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30404341-T-C

http://identifiers.org/hco/3/GRCh38#194669991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30404354-C-A

194670002-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 30404365-A-T

194670028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 30404391-T-A

194670073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30404436-A-G

194670127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30404490-T-G

194670155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30404518-G-A

194670185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30404552-G-A

194670185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30404552-G-T

194670197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30404564-C-G

194670287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30404743-C-T

194670289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30404745-C-T

194670290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30404746-G-A

194670522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30404945-G-A

194670739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30405163-G-C

194670833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30405204-T-A

194670858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30405229-T-C

194670864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30405240-G-C

http://identifiers.org/hco/3/GRCh38#194670895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30405286-C-A

194670913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30405304-C-G

194670913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30405304-C-T

194671171-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30405462-T-A

http://identifiers.org/hco/3/GRCh38#194671288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30405551-A-C

194671378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30405620-G-T

194671406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30405635-C-T

194671524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30405712-C-G

194671524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30405712-C-T

194671645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30405810-G-A

194671742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30406008-T-C

194671801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30406070-T-C

http://identifiers.org/hco/3/GRCh38#194671834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30406105-C-A

194671834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30406105-C-G

194671834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30406105-C-T

194671910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30406147-A-T

194671961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30406167-G-A

194671961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30406167-G-T

194671966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30406172-G-A

194671966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30406172-G-T

194672085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 30406277-G-A

194672085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 30406277-G-C

194672085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 30406277-G-T

194672104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 30406296-T-C

194672104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 30406296-T-G

194672150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30406342-T-C

194672150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30406342-T-G

194672157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30406349-G-A

194672157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30406349-G-T

http://identifiers.org/hco/3/GRCh38#194672201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30406390-C-A

194672201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: non coding transcript exon variant
orthologous variants: 30406390-C-T

194672206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: non coding transcript exon variant
orthologous variants: 30406395-A-G

http://identifiers.org/hco/3/GRCh38#194672230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30406419-C-A

194672230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: non coding transcript exon variant
orthologous variants: 30406419-C-G

194672230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: non coding transcript exon variant
orthologous variants: 30406419-C-T

http://identifiers.org/hco/3/GRCh38#194672242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30406431-C-A

194672242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: non coding transcript exon variant
orthologous variants: 30406431-C-T

194672286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: non coding transcript exon variant
orthologous variants: 30406477-A-G

194672295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: non coding transcript exon variant
orthologous variants: 30406486-G-A

194672295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: non coding transcript exon variant
orthologous variants: 30406486-G-C

194672295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: non coding transcript exon variant
orthologous variants: 30406486-G-T

194672310-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: non coding transcript exon variant
orthologous variants: 30406501-T-A

194672310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: non coding transcript exon variant
orthologous variants: 30406501-T-C

194672310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: non coding transcript exon variant
orthologous variants: 30406501-T-G

http://identifiers.org/hco/3/GRCh38#194672334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30406525-C-A

194672334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: non coding transcript exon variant
orthologous variants: 30406525-C-T

http://identifiers.org/hco/3/GRCh38#194672373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#30406565-A-C

194672373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25652
most severe consequence: non coding transcript exon variant
orthologous variants: 30406565-A-G