9019717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109397136-T-A

9019732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109397151-T-C

9019847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109397356-T-C

9020020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109397544-T-C

9020342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109397808-G-T

http://identifiers.org/hco/11/GRCh38#9020445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109397927-C-A

9020445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109397927-C-G

9020445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109397927-C-T

9020501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109397983-G-T

9020506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109397988-G-A

http://identifiers.org/hco/11/GRCh38#9020730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109398188-C-A

9020730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109398188-C-T

http://identifiers.org/hco/11/GRCh38#9020778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109398208-C-A

9020778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109398208-C-G

9020778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109398208-C-T

9020837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109398255-G-T

9020919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109398336-T-A

9020919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109398336-T-C

9020945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109398362-G-A

9020960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109398375-G-A

9020960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109398375-G-T

9020979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109398395-A-T

http://identifiers.org/hco/11/GRCh38#9020986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109398402-C-A

9020986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109398402-C-G

9020986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109398402-C-T

http://identifiers.org/hco/11/GRCh38#9021277-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109398691-A-C

http://identifiers.org/hco/11/GRCh38#9021386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109398802-A-C

9021501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109398913-T-G

9021732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109399679-T-C

9021756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109399703-G-T

9021773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109399719-G-A

9021773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109399719-G-T

9021823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109399733-T-C

http://identifiers.org/hco/11/GRCh38#9021912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109399817-C-A

9021954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 109399859-C-T

9021961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 109399866-G-A

9021969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109399874-G-A

9022003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109399907-C-G

9022003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109399907-C-T

9022019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109399923-A-G

9022535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109400375-C-T

http://identifiers.org/hco/11/GRCh38#9022577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109400416-C-A

9022588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109400426-T-C

9022612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109400450-C-T

9022661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109400489-C-G

9022661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109400489-C-T

9022696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109400524-T-A

http://identifiers.org/hco/11/GRCh38#9022703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109400531-C-A

9022703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109400531-C-T

9022740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109400563-T-C

http://identifiers.org/hco/11/GRCh38#9022775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109400597-C-A

http://identifiers.org/hco/11/GRCh38#9022788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109400610-C-A

9022793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109400615-G-A

http://identifiers.org/hco/11/GRCh38#9022798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109400620-C-A

9023200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109401024-G-A

9023230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109401054-T-C

9023363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109401176-T-C

9023445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109401842-C-T

9023457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109401854-G-C

http://identifiers.org/hco/11/GRCh38#9024131-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109402403-A-C

9024168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109402450-A-T

9024182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109402464-C-T

9024210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109402491-G-A

9024210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109402491-G-T

http://identifiers.org/hco/11/GRCh38#9024259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109402575-C-A

9024259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109402575-C-T

9024269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109402585-A-G

9024398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109402691-A-G

9024432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109402717-G-T

9024444-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109402728-T-G

9024448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109402732-A-G

9024628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109402893-C-G

9024891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109403122-T-G

9025230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109403266-C-G

9025272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109403308-A-T

9025311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109403362-G-A

9025326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109403377-G-A

http://identifiers.org/hco/11/GRCh38#9025366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109403455-C-A

9025366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109403455-C-G

http://identifiers.org/hco/11/GRCh38#9025368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109403457-C-A

9025483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109403567-G-A

9025483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109403567-G-T

9025529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109403616-A-G

9025594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109403682-G-T

9025630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109403717-T-C

9025639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109403726-G-A

9025877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109403987-G-C

http://identifiers.org/hco/11/GRCh38#9025896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109404006-C-A

http://identifiers.org/hco/11/GRCh38#9025972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109404080-C-A

9025972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109404080-C-T

9025973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109404081-A-G

9026786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109404668-T-C

9026951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109404797-T-G

http://identifiers.org/hco/11/GRCh38#9027278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109405163-C-A

9027536-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 109405422-T-A

9027599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109405487-G-C

9027608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109405496-G-A

http://identifiers.org/hco/11/GRCh38#9027615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109405503-C-A

9027615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109405503-C-T

http://identifiers.org/hco/11/GRCh38#9027617-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109405505-A-C

9027626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109405514-T-C

9027626-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109405514-T-G

http://identifiers.org/hco/11/GRCh38#9027636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109405520-C-A

9027636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109405520-C-T

9027677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109405542-T-A

9027690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109405556-G-A

9027690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109405556-G-T

http://identifiers.org/hco/11/GRCh38#9027706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109405575-C-A

9027706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109405575-C-G

9027706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109405575-C-T

9027715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109405581-C-T

9028383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109406155-G-T

9028651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109406388-T-C

9028749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109406495-G-A

9029011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109406874-A-G

9029327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109407051-A-G

9029469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109407162-C-T

9029608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109407271-G-A

http://identifiers.org/hco/11/GRCh38#9029749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109407483-C-A

9029749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109407483-C-T

9029775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109407509-A-G

http://identifiers.org/hco/11/GRCh38#9029830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109407568-C-A

http://identifiers.org/hco/11/GRCh38#9029837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109407575-C-A

9029837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109407575-C-G

9029837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109407575-C-T

9030129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109407823-G-A

9030129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109407823-G-T

9030151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109407845-T-C

9030160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109407854-G-A

9030160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109407854-G-T

9030181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109407875-T-C

9030219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109407913-G-A

9030366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109407998-A-T

9030370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109408002-G-T

9030416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109408041-G-T

9030420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109408045-T-C

9030425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109408050-G-T

http://identifiers.org/hco/11/GRCh38#9030429-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109408053-A-C

9030429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109408053-A-G

http://identifiers.org/hco/11/GRCh38#9030435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109408059-A-C

9030439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109408063-G-A

9030439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109408063-G-C

9030439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109408063-G-T

9030464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109408080-G-T

http://identifiers.org/hco/11/GRCh38#9030467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109408083-A-C

9030474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109408092-A-G

9030496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109408114-G-C

9030658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109408195-G-A

9030658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109408195-G-T

http://identifiers.org/hco/11/GRCh38#9030681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109408205-C-A

http://identifiers.org/hco/11/GRCh38#9030723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109408254-C-A

9030723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109408254-C-T

9030724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109408255-A-G

9030964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109408490-G-T

9030974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109408500-T-C

http://identifiers.org/hco/11/GRCh38#9031009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109408535-C-A

9031014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109408540-T-A

9031014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109408540-T-C

http://identifiers.org/hco/11/GRCh38#9031112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109408627-C-A

9031112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109408627-C-T

http://identifiers.org/hco/11/GRCh38#9031136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109408651-C-A

9031199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109408693-G-A

9031205-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109408694-T-G

http://identifiers.org/hco/11/GRCh38#9031209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109408698-C-A

9031209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109408698-C-T

9031299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109408811-A-G

9033477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109409638-G-T

9033491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109409652-G-A

9033491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109409652-G-T

9033506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109409663-G-T

9033531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109409688-G-A

9033531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109409688-G-C

9033531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109409688-G-T

9033556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109409714-T-G

9033584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109409750-T-C

9033591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109409757-T-C

9033612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109409778-G-C

9033634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 109409800-T-C

9033639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 109409805-C-T

9033647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 109409813-A-G

9033647-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 109409813-A-T

9033667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 109409833-G-A

9033707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 109409873-T-G

9033744-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 109409910-T-A

9033780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 109409946-C-T

9033832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109409998-A-G

9033846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109410012-A-T

9033854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109410020-G-A

9033854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109410020-G-T

9033867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109410033-A-G

9033928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109410097-A-G

9033928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109410097-A-T

9034001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109410143-C-T

9034020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109410162-A-G

9034139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109410261-G-A

9034213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109410466-G-A

9034302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109410553-G-A

9034424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109410674-T-C

9035526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109411294-C-T

9035654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109411377-G-C

http://identifiers.org/hco/11/GRCh38#9035780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109411428-C-A

9035780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109411428-C-T

9036334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109411918-C-T

9036395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109411979-G-A

9036425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109412007-A-G

9036604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109412177-A-G

9036688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109412260-A-T

9036938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109412455-C-T

9037289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109412776-G-A

9037463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109412974-A-T

9037743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109413258-G-A

9037961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109413483-A-G

9043503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109418690-G-A

9043503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109418690-G-T

9045525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109421780-C-T

http://identifiers.org/hco/11/GRCh38#9045657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109421881-C-A

9045657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109421881-C-G

9045702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109421940-A-G

9045767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109421985-T-C

9046820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109422642-T-A

9046856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109422676-G-A

9047249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109423864-A-G

9047263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109423878-G-T

9047422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 109424038-G-A

http://identifiers.org/hco/11/GRCh38#9047471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109424087-C-A

9047471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 109424087-C-G

9047471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 109424087-C-T

9047595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109424212-G-A

9047615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109424228-G-T

9047703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109424284-G-A

9047703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109424284-G-T

9047740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109424321-T-C

9047829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109424404-G-A

9047829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109424404-G-T

9047864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109424447-G-T

9047907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109424490-G-A

http://identifiers.org/hco/11/GRCh38#9048205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109424784-A-C

9048205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109424784-A-T

http://identifiers.org/hco/11/GRCh38#9048325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109424885-C-A

9048342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109424902-G-A

9048391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109424948-G-A

9048397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109424998-C-T

9048471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109425084-C-T

9048480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109425093-G-A

9050213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109427679-A-T

9050329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109427782-T-C

9050359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109427812-G-T

9050394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109428057-G-A

9050394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109428057-G-T

9050412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109428075-T-C

9050546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109428180-G-A

9050558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109428192-C-G

9050568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109428204-G-A

9050568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109428204-G-T

http://identifiers.org/hco/11/GRCh38#9050611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109428247-A-C

9050613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 109428249-T-C

9050699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 109428335-T-C

9050724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109428360-C-T

9050784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109428418-G-T

9050787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109428421-G-T

http://identifiers.org/hco/11/GRCh38#9050829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109428463-C-A

9050829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109428463-C-T

http://identifiers.org/hco/11/GRCh38#9050837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109428468-C-A

9050837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109428468-C-G

9050837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109428468-C-T

9050846-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109428483-T-A

9050846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109428483-T-G

9051094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109428611-C-T

9051350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109428652-A-T

http://identifiers.org/hco/11/GRCh38#9051466-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109428743-A-C

9051466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109428743-A-G

9051475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109428752-G-A

9051475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109428752-G-T

9052140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109429384-A-G

9052484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109429748-G-A

http://identifiers.org/hco/11/GRCh38#9052676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109429939-C-A

9052676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109429939-C-T

http://identifiers.org/hco/11/GRCh38#9052679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109429942-C-A

9052682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109429945-C-G

9052721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109429982-G-A

9052721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109429982-G-T

9052837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 109430092-C-T

http://identifiers.org/hco/11/GRCh38#9052911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109430169-C-A

9052911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109430169-C-T

http://identifiers.org/hco/11/GRCh38#9052914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109430172-C-A

http://identifiers.org/hco/11/GRCh38#9053071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109430309-C-A

9053071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109430309-C-G

9053071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109430309-C-T

9053124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 109430360-A-G

9053193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 109430429-T-G

9053236-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109430474-A-T

9053266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109430504-G-A

9053266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109430504-G-T

http://identifiers.org/hco/11/GRCh38#9053303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109430534-C-A

9053426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109430660-G-C

9053482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109430716-T-C

9053565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109430796-G-A

9053565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109430796-G-C

9053565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109430796-G-T

http://identifiers.org/hco/11/GRCh38#9053583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109430814-C-A

9053583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109430814-C-T

9053589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109430823-G-A

9053922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109431130-G-A

http://identifiers.org/hco/11/GRCh38#9053938-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109431148-A-C

9054289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109431223-A-G

9054440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109431293-G-A

9054517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109431368-C-T

9054518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109431369-C-G

9054528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109431379-G-A

http://identifiers.org/hco/11/GRCh38#9054694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109431539-C-A

9055211-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109431707-T-G

9055426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109431902-G-A

9055519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109431987-C-G

9055522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109431990-C-T

9055583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109432045-A-G

9055748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109432182-C-T

9055770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109432193-C-T

9055946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109432369-C-T

9055983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109432403-A-G

9055983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109432403-A-T

9056037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109432452-A-G

9056076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109432490-A-G

9056393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109433371-A-G

9056568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109433546-A-G

9056573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109433551-C-T

http://identifiers.org/hco/11/GRCh38#9056652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109433616-C-A

9056652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109433616-C-T

9056698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109433640-G-T

9056874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109433779-G-A

9056975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109434121-C-G

http://identifiers.org/hco/11/GRCh38#9057091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109434238-C-A

9057091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109434238-C-T

http://identifiers.org/hco/11/GRCh38#9057118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109434265-C-A

9057367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109434513-T-C

http://identifiers.org/hco/11/GRCh38#9057385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109434531-C-A

http://identifiers.org/hco/11/GRCh38#9057745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109434997-C-A

9057810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109435080-G-A

http://identifiers.org/hco/11/GRCh38#9057992-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109435349-A-C

http://identifiers.org/hco/11/GRCh38#9058996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109435915-C-A

http://identifiers.org/hco/11/GRCh38#9059041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109435959-C-A

9059068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109435987-T-C

9059076-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109435995-T-A

http://identifiers.org/hco/11/GRCh38#9059173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109436066-C-A

9059192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109436086-A-G

9059192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109436086-A-T

9059194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109436088-T-C

9059209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109436102-G-T

http://identifiers.org/hco/11/GRCh38#9059274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109436172-C-A

9059274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109436172-C-T

9059346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 109436244-G-A

http://identifiers.org/hco/11/GRCh38#9059546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109436415-C-A

9059663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109436514-T-C

9059699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109436550-G-A

9059748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109436603-G-A

9059748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109436603-G-C

9059748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109436603-G-T

http://identifiers.org/hco/11/GRCh38#9059763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109436618-C-A

9059763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109436618-C-G

http://identifiers.org/hco/11/GRCh38#9059800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109436656-C-A

9059817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109436661-G-A

9059817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109436661-G-T

9059833-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109436677-T-G

9059868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109436712-A-G

9060030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109436884-T-C

9060068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109436921-T-C

9060087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109436940-T-C

9060240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109437091-T-C

9060374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 109437245-G-A

9060374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 109437245-G-C

9060374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 109437245-G-T

9060375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 109437246-G-A

9060375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 109437246-G-T

9060382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109437253-A-G

9060382-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109437253-A-T

9060383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109437254-G-T

9060433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 109437312-G-A

9060647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109437525-T-C

9060654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109437532-G-T

9060879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109437719-G-A

9061163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109437920-A-G

9064796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109441061-A-G

http://identifiers.org/hco/11/GRCh38#9064897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109441151-C-A

9064897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109441151-C-T

9065057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109441309-G-T

9065081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109441333-G-T

9065174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109441452-G-A

9065174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109441452-G-T

9065270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109441539-G-C

9065270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109441539-G-T

9065284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109441553-G-T

9065304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109441591-T-A

9065353-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109441636-T-A

9065598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109442108-A-G

9065640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109442146-C-T

9065655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109442161-T-A

9065761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109442267-T-C

http://identifiers.org/hco/11/GRCh38#9065764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109442270-C-A

9065764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109442270-C-T

9065774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109442280-T-C

http://identifiers.org/hco/11/GRCh38#9065788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109442294-C-A

http://identifiers.org/hco/11/GRCh38#9065822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109442322-C-A

9065822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 109442322-C-G

9065881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109442376-A-G

http://identifiers.org/hco/11/GRCh38#9065979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109442475-C-A

9065979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 109442475-C-T

9066015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109442509-T-C

http://identifiers.org/hco/11/GRCh38#9066068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109442562-C-A

9066068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109442562-C-T

http://identifiers.org/hco/11/GRCh38#9066100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109442599-C-A

9066100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109442599-C-T

http://identifiers.org/hco/11/GRCh38#9066105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109442604-A-C

9066119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109442620-G-A

9066313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109442785-C-T

9066319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109442791-G-A

9066353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109442802-G-A

9066409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109442853-T-A

9066464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109442908-G-A

9066488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 109442932-G-T

9066568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109442999-G-A

9066568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109442999-G-T

9066630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109443035-T-C

http://identifiers.org/hco/11/GRCh38#9066868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109443253-C-A

9066868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109443253-C-T

http://identifiers.org/hco/11/GRCh38#9066917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109443462-C-A

9066927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109443472-A-G

http://identifiers.org/hco/11/GRCh38#9066956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109443501-C-A

9066956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109443501-C-T

9069271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, undefined
orthologous variants: 109446048-G-A

9069271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, undefined
orthologous variants: 109446048-G-T

http://identifiers.org/hco/11/GRCh38#9069275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109446052-C-A

9069275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, undefined
orthologous variants: 109446052-C-T

9069283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, undefined
orthologous variants: 109446065-T-G

9069290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, undefined
orthologous variants: 109446072-G-T

9069298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109446080-G-T

9069356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, undefined
orthologous variants: 109446116-T-C

9069583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109446324-A-G

9069600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109446340-G-T

9070548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109448149-A-G

http://identifiers.org/hco/11/GRCh38#9070854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109448428-C-A

9070947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109448534-G-T

http://identifiers.org/hco/11/GRCh38#9071009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109448595-C-A

9071393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109448969-C-T

9071644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109449219-T-C

9071749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109449307-A-G

9071929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109449481-G-A

9071994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109449534-A-G

9072354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109449699-G-A

9072989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109450159-A-G

9073541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109450640-T-A

9073825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109450923-T-A

9073942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109451053-C-T

9073992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109451118-C-T

9074187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109451318-G-A

9074194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109451325-C-G

9074273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109451404-C-G

http://identifiers.org/hco/11/GRCh38#9074350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109451479-C-A

9074527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: synonymous variant
orthologous variants: 109451687-C-T

9075479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109452341-A-G

9075728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109452569-C-T

9076155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109452936-C-T

9076170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109452953-G-T

9076265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109453043-G-A

9076324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109453101-G-A

9076423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109453192-C-T

9076437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109453206-C-G

9076540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109453322-T-C

9076579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109453357-G-T

9076615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109453396-T-C

9076816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, undefined
orthologous variants: 109453586-T-C

9076882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, undefined
orthologous variants: 109453649-C-G

9076882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, undefined
orthologous variants: 109453649-C-T

9076883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, undefined
orthologous variants: 109453650-G-A

9076883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, undefined
orthologous variants: 109453650-G-T

9077346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109453998-T-C

9077394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109454038-G-A

9077474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109454105-C-T

9077535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109454143-G-A

9077743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109454773-A-G

9077966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109454949-T-C

9078083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109455038-G-A

9078183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109455106-C-G

9078279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109455203-G-A

http://identifiers.org/hco/11/GRCh38#9078299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109455223-C-A

9078299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, undefined
orthologous variants: 109455223-C-T

9078411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109455302-G-A

9078484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109455782-A-G

9078535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109455831-A-G

9078685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109455908-C-T

9078840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109456053-G-A

9078844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109456057-G-A

9079205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109456433-G-C

http://identifiers.org/hco/11/GRCh38#9079213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109456449-A-C

9079213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109456449-A-G

9079260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109456526-T-C

9079268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109456575-G-A

9079268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109456575-G-T

http://identifiers.org/hco/11/GRCh38#9079292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109456649-C-A

9079292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109456649-C-T

9079301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109456658-G-C

9079301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109456658-G-T

9079315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109456672-G-C

9079349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109456704-G-A

9079374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron variant
orthologous variants: 109456718-C-T

9079489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109456833-C-T

9079506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109456850-A-G

9079506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109456850-A-T

9079540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109456884-G-A

9079541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109456885-G-A

9079541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109456885-G-C

9079541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109456885-G-T

9079651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109456966-T-C

9079704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109457019-C-T

9088064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109461995-G-A

http://identifiers.org/hco/11/GRCh38#9088146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109462066-C-A

9088169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109462094-C-T

9088197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109462120-T-C

9088666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109462445-G-A

9088666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109462445-G-C

9088713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109462492-C-T

9088801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109462555-A-T

http://identifiers.org/hco/11/GRCh38#9088931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109462664-C-A

9088931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109462664-C-T

9088955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109462689-G-C

9089226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109462940-T-G

9089261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109462971-C-T

http://identifiers.org/hco/11/GRCh38#9089567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109463196-A-C

9089567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109463196-A-G

9089567-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109463196-A-T

http://identifiers.org/hco/11/GRCh38#9089617-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109463228-A-C

9089617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109463228-A-G

http://identifiers.org/hco/11/GRCh38#9089632-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109463243-A-C

9089632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109463243-A-G

9089632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109463243-A-T

http://identifiers.org/hco/11/GRCh38#9089634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109463245-A-C

9089664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109463269-G-C

9089762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109463367-G-A

9089896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109463518-G-C

9089896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109463518-G-T

9089904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109463526-T-A

9089904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109463526-T-C

9089955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109463587-G-C

9089955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109463587-G-T

9090050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109463681-C-T

9090128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109463772-G-A

9090128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109463772-G-T

9090206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109463849-T-C

9090730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109464123-C-T

9090789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109464183-T-G

9091080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109464431-C-G

9091121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109464455-G-A

9091121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109464455-G-C

9091349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109464623-T-A

9091349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109464623-T-C

9091349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109464623-T-G

http://identifiers.org/hco/11/GRCh38#9091373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109464645-C-A

9091373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109464645-C-G

9091373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109464645-C-T

http://identifiers.org/hco/11/GRCh38#9091535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109464800-C-A

9091535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109464800-C-G

9091535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109464800-C-T

9091549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109464806-G-A

9091549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109464806-G-T

9091577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109464830-G-A

9091577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109464830-G-T

9091597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109464850-T-C

9091597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109464850-T-G

http://identifiers.org/hco/11/GRCh38#9091609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109464862-C-A

9091609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109464862-C-T

http://identifiers.org/hco/11/GRCh38#9091620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109464872-C-A

9091620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109464872-C-T

http://identifiers.org/hco/11/GRCh38#9091630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109464882-C-A

9091762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109464971-G-A

9091783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109464992-T-C

9091789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109464998-G-A

9091789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109464998-G-C

9091922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109465068-G-T

9092156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109465256-C-T

9092159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109465259-C-T

9092571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109465610-C-G

9092688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109465731-T-C

9092707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109465753-G-A

9092746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109465794-C-G

9093142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109466212-C-T

9093151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109466222-C-T

9093252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109466323-C-T

9093703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109466790-G-A

9093703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109466790-G-C

9093940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109466974-C-G

9094062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109467049-C-G

http://identifiers.org/hco/11/GRCh38#9094291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109467246-C-A

9108108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109471274-T-C

9108139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109471295-G-A

9108214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109471370-G-A

http://identifiers.org/hco/11/GRCh38#9108667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109472063-A-C

9108674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109472070-T-C

http://identifiers.org/hco/11/GRCh38#9110286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109474743-C-A

9110304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109474761-A-T

9110469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109474873-C-G

9110823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109475185-G-A

9110903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109475270-C-T

9121565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109479825-T-A

9121566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109479826-G-A

9121644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109479902-G-A

9121705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109479959-A-G

9124588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109482080-A-G

9125332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109482448-G-T

9125338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109482454-G-A

http://identifiers.org/hco/11/GRCh38#9126242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109483101-A-C

http://identifiers.org/hco/11/GRCh38#9126287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109483147-C-A

9126287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109483147-C-G

http://identifiers.org/hco/11/GRCh38#9127047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109484019-C-A

9127047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109484019-C-T

9130037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109487231-C-T

9130106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109487290-A-G

9131066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109488761-G-C

9131269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109488841-T-C

9131433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109489061-C-T

9131697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109489305-T-C

http://identifiers.org/hco/11/GRCh38#9131827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109489495-C-A

9131891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109489569-G-A

9131975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109489652-T-A

9131975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109489652-T-C

9132278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109489903-T-C

9132285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109489910-G-A

9132394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109490008-G-T

9132743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109490335-A-G

9137278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109490734-G-A

9137295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109490748-G-C

9137306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109490753-G-A

9137307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109490754-G-T

9137365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109490806-G-A

9137408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109490852-C-T

9137440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109490884-G-A

9137532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109490972-G-A

9137586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109491023-A-G

http://identifiers.org/hco/11/GRCh38#9137814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109491871-C-A

9137814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109491871-C-T

9137817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109491874-G-T

9137844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 109491901-T-C

9137857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: non coding transcript exon variant
orthologous variants: 109491915-C-T

http://identifiers.org/hco/11/GRCh38#9137966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109492002-C-A

9137966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 109492002-C-T

9138002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 109492045-G-T

http://identifiers.org/hco/11/GRCh38#9138065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109492104-C-A

9138065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: non coding transcript exon variant
orthologous variants: 109492104-C-T

9138068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: non coding transcript exon variant
orthologous variants: 109492107-G-C

9138068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: non coding transcript exon variant
orthologous variants: 109492107-G-T

9138105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: non coding transcript exon variant
orthologous variants: 109492154-G-C

9138105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30425
most severe consequence: non coding transcript exon variant
orthologous variants: 109492154-G-T