http://identifiers.org/hco/12/GRCh38#47973072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97873593-C-A

47973072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: 3 prime UTR variant
orthologous variants: 97873593-C-T

47973123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: 3 prime UTR variant
orthologous variants: 97873641-A-G

47973526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97874040-C-T

47973669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97874161-C-T

47973805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97874283-C-T

47973926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97874405-C-T

47973970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97874449-A-G

47973983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97874462-G-C

47973983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97874462-G-T

47973993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97874473-T-A

http://identifiers.org/hco/12/GRCh38#47974082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97874516-C-A

47974082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 97874516-C-T

47974131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97874565-G-A

http://identifiers.org/hco/12/GRCh38#47974146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97874580-C-A

47974314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97874748-G-A

47974314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97874748-G-T

47974349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97874782-G-A

47974349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97874782-G-C

47974405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97874840-C-G

http://identifiers.org/hco/12/GRCh38#47974413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97874848-C-A

http://identifiers.org/hco/12/GRCh38#47974559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97874958-C-A

47974559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97874958-C-G

47974559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97874958-C-T

47974569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97874968-A-T

47974636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97875032-G-C

47974636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97875032-G-T

47974708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97875096-G-T

47974747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97875135-C-T

47974822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97875210-G-A

47974822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97875210-G-C

http://identifiers.org/hco/12/GRCh38#47975005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97875347-C-A

47975005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97875347-C-T

47975224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97875493-G-A

47975224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97875493-G-T

47975235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97875504-G-T

47975263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97875541-C-T

47975265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97875543-A-G

47975265-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97875543-A-T

47975387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97875672-G-A

47975432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97875717-G-A

47975435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97875720-A-G

47975480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97875765-G-A

http://identifiers.org/hco/12/GRCh38#47975632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97875917-C-A

47975717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97875995-G-A

47975717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97875995-G-T

47975735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97876007-G-A

47975735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97876007-G-C

47975735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97876007-G-T

47975874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97876141-G-T

http://identifiers.org/hco/12/GRCh38#47975939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97876195-C-A

47975939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97876195-C-T

47975943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97876199-G-T

http://identifiers.org/hco/12/GRCh38#47976074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97876330-C-A

47976090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97876349-T-C

47976400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97876639-G-T

47976506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 97876751-T-C

47976634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97876878-G-A

http://identifiers.org/hco/12/GRCh38#47976648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97876892-A-C

47976648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97876892-A-G

http://identifiers.org/hco/12/GRCh38#47976672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97876896-A-C

47976672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97876896-A-G

47976765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97876987-G-A

47976869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97877103-C-G

http://identifiers.org/hco/12/GRCh38#47976939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97877173-C-A

47976939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97877173-C-T

47976973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97877195-C-G

47976973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97877195-C-T

47976988-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97877210-A-T

47977105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97877269-G-T

http://identifiers.org/hco/12/GRCh38#47977210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97877380-C-A

47977210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97877380-C-T

47977470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97877662-A-G

47977474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97877666-G-A

47977474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97877666-G-T

47977550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97877709-G-A

47977621-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97877777-T-A

47977621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97877777-T-C

47977645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97877801-G-A

http://identifiers.org/hco/12/GRCh38#47977735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97877878-C-A

http://identifiers.org/hco/12/GRCh38#47977767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97877906-C-A

47977767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97877906-C-T

47977773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97877912-G-T

47977783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97877922-T-C

47977797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97877934-T-C

http://identifiers.org/hco/12/GRCh38#47977965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97877996-C-A

47977965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97877996-C-T

http://identifiers.org/hco/12/GRCh38#47977974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97878005-C-A

47977974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97878005-C-G

47978129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97878146-G-A

47978147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97878164-G-A

47978147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97878164-G-C

47978147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97878164-G-T

http://identifiers.org/hco/12/GRCh38#47978182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97878202-C-A

47978189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97878211-G-T

47978222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97878244-G-A

47978222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97878244-G-T

http://identifiers.org/hco/12/GRCh38#47978284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97878322-C-A

47978309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97878347-A-G

47978368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97878406-G-A

47978471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97878507-C-T

47978475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97878511-G-A

47978475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97878511-G-T

http://identifiers.org/hco/12/GRCh38#47978509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97878544-C-A

47978515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97878550-C-G

http://identifiers.org/hco/12/GRCh38#47978521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97878555-C-A

http://identifiers.org/hco/12/GRCh38#47978788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97878797-C-A

47978788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97878797-C-T

http://identifiers.org/hco/12/GRCh38#47978803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97878809-C-A

47978803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97878809-C-T

http://identifiers.org/hco/12/GRCh38#47978820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97878826-A-C

47978998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97878927-C-T

47979073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97879005-C-T

47979179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97879110-G-A

47979451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97879324-G-C

47979451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97879324-G-T

47979556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97879441-A-G

47979619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97879516-T-A

47979619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97879516-T-C

47979619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97879516-T-G

47979667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97879567-G-A

47979667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97879567-G-T

47979719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97879616-C-T

47979963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97879859-G-A

47979963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97879859-G-T

47979994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97879870-A-G

47980021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97879897-G-A

47980021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97879897-G-T

47980138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97880012-T-C

47980148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97880028-A-G

47980198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97880073-G-T

http://identifiers.org/hco/12/GRCh38#47980203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97880078-C-A

47980441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97880309-G-C

47980441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97880309-G-T

47980481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97880353-G-A

47980481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97880353-G-T

47980572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97880428-A-G

47980617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97880473-G-A

47980617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97880473-G-T

http://identifiers.org/hco/12/GRCh38#47980709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97880564-C-A

47980709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97880564-C-G

47980729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97880576-C-T

47980797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97880663-G-A

47980797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97880663-G-C

47980797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97880663-G-T

47980833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97880687-T-C

47980867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97880748-G-A

47980951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97880833-A-G

47980960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97880842-A-G

47981005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97880880-C-T

47981047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97880915-G-A

47981047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97880915-G-T

47981081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97880957-A-G

47981092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97880966-G-A

47981092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97880966-G-T

47981111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97880983-G-A

47981111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97880983-G-T

47981116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97880987-G-C

47981218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97881061-G-A

47981218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97881061-G-T

47981370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97881146-T-C

47981429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97881182-A-G

http://identifiers.org/hco/12/GRCh38#47981547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97881311-C-A

47981547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97881311-C-T

47981666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97881408-C-T

47981742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97881480-G-A

47981742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97881480-G-T

http://identifiers.org/hco/12/GRCh38#47981812-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97881569-A-C

47981812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97881569-A-G

47981837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 97881594-G-A

47981909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97881681-G-T

47981914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97881686-T-C

47981914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97881686-T-G

47981946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 97881717-C-T

47981957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97881729-T-C

47981974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97881746-C-T

47981990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97881762-C-T

47982038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97881810-T-C

47982165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 97881899-G-A

47982223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97881954-T-C

47982223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97881954-T-G

47982309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97882037-G-A

47982309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97882037-G-T

47982354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97882075-G-A

47982354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97882075-G-T

47982544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97882285-G-A

47982544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97882285-G-C

47982586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97882327-G-A

47982606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97882347-C-T

47982614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 97882355-G-A

http://identifiers.org/hco/12/GRCh38#47982660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97882412-A-C

http://identifiers.org/hco/12/GRCh38#47982662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97882414-C-A

http://identifiers.org/hco/12/GRCh38#47982693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97882445-C-A

47982693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97882445-C-G

http://identifiers.org/hco/12/GRCh38#47982694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97882446-C-A

47982727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97882467-A-T

47982778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97882528-T-C

http://identifiers.org/hco/12/GRCh38#47982827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97882580-A-C

47982875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97882628-G-A

47982875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97882628-G-C

47982911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97882664-G-A

47982911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97882664-G-C

47983004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97882772-G-A

47983029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97882822-G-C

47983258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883056-G-A

47983258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883056-G-T

47983274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883072-A-T

47983348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883133-C-T

47983378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 97883156-T-C

47983465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883243-C-T

47983481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883259-C-T

47983485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883263-C-T

47983532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883310-G-A

47983532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883310-G-T

47983590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883358-G-A

47983590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883358-G-T

47983596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883364-G-A

47983596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883364-G-T

47983597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883365-G-A

47983597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883365-G-T

47983633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883394-G-T

http://identifiers.org/hco/12/GRCh38#47983636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97883397-C-A

47983636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883397-C-T

47983776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97883536-A-G

47983776-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97883536-A-T

47983808-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97883552-A-T

http://identifiers.org/hco/12/GRCh38#47983940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97883647-C-A

47983940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883647-C-T

http://identifiers.org/hco/12/GRCh38#47983984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97883675-C-A

47984006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883697-A-G

47984063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883722-T-A

47984063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883722-T-C

47984063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883722-T-G

47984064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883723-G-A

47984064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883723-G-C

47984064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883723-G-T

http://identifiers.org/hco/12/GRCh38#47984162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97883819-A-C

47984162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883819-A-G

47984169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883826-T-A

47984169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883826-T-C

47984193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883852-A-G

47984225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883877-G-A

47984225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883877-G-T

http://identifiers.org/hco/12/GRCh38#47984266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97883917-C-A

47984266-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883917-C-G

http://identifiers.org/hco/12/GRCh38#47984280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97883930-C-A

47984280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883930-C-T

47984284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883934-T-C

47984284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883934-T-G

47984301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97883951-C-T

47984451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97884096-G-A

47984451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97884096-G-C

47984451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97884096-G-T

47984460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97884105-A-G

47984461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97884106-C-G

http://identifiers.org/hco/12/GRCh38#47984508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97884152-C-A

http://identifiers.org/hco/12/GRCh38#47984514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97884158-C-A

http://identifiers.org/hco/12/GRCh38#47984597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97884240-A-C

47984597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 97884240-A-G

47984629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97884271-G-T

47984631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97884273-G-A

47984631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97884273-G-T

47984640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97884282-G-A

47984640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97884282-G-T

47984644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97884286-G-A

47984644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97884286-G-T

47984686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97884323-G-A

47984686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97884323-G-T

47984719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97884357-A-G

47984753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97884392-A-G

47984934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97884572-A-G

47984964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97884592-G-T

47985076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97884704-A-G

47985164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97884790-G-A

47985164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97884790-G-T

47985188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97884817-A-G

47985229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97884854-T-A

47985261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97884886-C-T

47985343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97884983-G-T

47985373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97885007-C-T

http://identifiers.org/hco/12/GRCh38#47985624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97885279-C-A

47985691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97885344-G-C

47985691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97885344-G-T

47985723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97885361-C-T

47985793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97885431-C-T

47985824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 97885462-T-C

47985844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97885484-G-T

47985904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 97885541-C-T

47985978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97885610-A-G

47985979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97885611-G-A

47985979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97885611-G-T

47986031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97885681-G-A

47986031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97885681-G-T

47986079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97885728-T-A

47986079-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97885728-T-G

47986080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97885729-G-A

47986080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97885729-G-T

47986084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97885733-T-C

http://identifiers.org/hco/12/GRCh38#47986105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97885756-C-A

47986121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97885774-C-T

47986122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97885775-G-A

47986130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97885783-G-C

47986214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97885863-G-T

47986267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97885919-A-G

47986267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97885919-A-T

http://identifiers.org/hco/12/GRCh38#47986271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97885923-C-A

47986313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97885944-T-C

47986315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97885946-G-A

http://identifiers.org/hco/12/GRCh38#47986319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97885949-C-A

47986319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97885949-C-G

47986372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97886001-A-G

http://identifiers.org/hco/12/GRCh38#47986426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97886055-C-A

47986426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97886055-C-T

47986429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97886058-G-A

47986429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97886058-G-T

47986559-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97886189-T-A

47986559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97886189-T-C

47986559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97886189-T-G

http://identifiers.org/hco/12/GRCh38#47986574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97886217-C-A

47986574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97886217-C-T

47986619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97886247-A-G

47986706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97886322-G-A

47986706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97886322-G-C

47986706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97886322-G-T

47986715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97886331-G-T

47986724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97886340-C-T

47986779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97886391-C-T

47986790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97886399-T-C

47986906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97886517-G-A

47986957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97886559-T-C

47987204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97886769-G-A

47987258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97886818-G-A

47987376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97886938-C-T

http://identifiers.org/hco/12/GRCh38#47987432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97886993-C-A

47987471-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97887034-A-T

47987478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97887041-G-C

47987478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97887041-G-T

47987707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 97887263-A-T

47987764-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97887298-T-G

47987767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97887301-T-C

47987786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97887318-G-T

47987787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97887319-G-A

47987787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97887319-G-T

http://identifiers.org/hco/12/GRCh38#47987813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97887337-A-C

47987849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97887370-G-A

47987849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97887370-G-T

http://identifiers.org/hco/12/GRCh38#47987858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97887379-C-A

47987858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97887379-C-T

47987944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97887456-T-C

47988280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97887805-C-T

47988326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97887907-A-G

http://identifiers.org/hco/12/GRCh38#47988339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97887920-A-C

47988428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 97888016-G-A

47988428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 97888016-G-T

47988491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97888080-T-C

47988491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97888080-T-G

47988808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97888391-G-A

47989050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97888591-A-G

47989181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97888746-A-G

47989299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97888865-A-G

47989310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97888878-G-A

http://identifiers.org/hco/12/GRCh38#47989342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97888918-C-A

47989342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97888918-C-T

47989426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97888974-G-A

47989426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97888974-G-T

47989453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97888999-C-G

47989658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97889154-T-A

47989658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97889154-T-C

http://identifiers.org/hco/12/GRCh38#47989684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97889166-C-A

47989684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97889166-C-T

47991483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97890479-C-T

47991569-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97890542-T-G

47991760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97890706-G-T

47991772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97890718-G-A

47991878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97890808-G-A

47991984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97890908-A-G

47992219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97891161-C-T

47992404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97891318-C-T

47992419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97891328-T-C

47992440-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97891349-T-A

47992440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97891349-T-C

47992547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97891413-A-G

47992562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97891427-T-G

47992563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97891428-A-G

47992573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97891438-G-A

47992696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97891554-C-T

47992713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97891571-G-T

47992740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97891631-G-A

47992740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97891631-G-T

47992761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97891761-T-A

47992761-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97891761-T-G

47992775-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97891787-A-T

47992843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97891863-G-A

47992843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97891863-G-T

47992844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97891864-C-T

47992911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: synonymous variant
orthologous variants: 97891931-A-G

47992959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97891979-C-T

47993069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97892041-G-T

47993070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97892042-G-A

47993070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97892042-G-T

47993077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97892049-C-T

47993116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97892070-G-A

47993116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97892070-G-C

47993140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97892091-G-A

47993189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97892127-G-C

47993270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97892206-A-G

47993391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97892340-C-T

47993444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97892408-G-T

47993447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97892411-T-C

47993467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: synonymous variant
orthologous variants: 97892434-C-T

47993596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97892558-G-T

47993618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97892584-G-T

47993623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97892589-G-A

47993623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97892589-G-T

http://identifiers.org/hco/12/GRCh38#47993631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97892597-C-A

47993723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97892675-G-C

47993723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97892675-G-T

47993726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97892678-C-T

47993894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97892833-T-A

47993979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97892882-A-G

47994057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97892960-A-G

47994069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97892972-T-C

http://identifiers.org/hco/12/GRCh38#47994166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97893057-C-A

47994166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97893057-C-T

47994177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97893068-C-T

47994296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97893148-T-C

47994297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97893149-G-A

47994297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97893149-G-T

47994347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97893172-C-G

47994347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97893172-C-T

47994349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97893174-G-A

47994349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97893174-G-T

47994358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97893183-G-A

47994358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97893183-G-C

http://identifiers.org/hco/12/GRCh38#47994573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97893363-C-A

47994573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97893363-C-G

47994573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97893363-C-T

http://identifiers.org/hco/12/GRCh38#47994601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97893391-C-A

47994601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97893391-C-T

47994611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97893401-A-G

47994620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97893409-G-A

47994620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97893409-G-C

47994929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97893690-C-T

47994960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97893720-C-T

47995255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 97893984-A-G

47995255-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 97893984-A-T

47995358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97894081-C-T

47995486-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97894191-T-G

47995513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97894218-G-C

47995550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97894244-C-G

http://identifiers.org/hco/12/GRCh38#47995561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97894255-C-A

47995603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97894273-C-G

47995615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97894285-G-T

47995669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97894336-A-G

47995669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97894336-A-T

47995670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97894337-G-A

47995716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: synonymous variant
orthologous variants: 97894376-A-G

47995734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: synonymous variant
orthologous variants: 97894394-A-T

47995782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97894442-A-G

47995881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: synonymous variant
orthologous variants: 97894535-A-G

47995939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97894595-G-A

47995939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97894595-G-T

47995943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97894599-G-T

47995958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97894613-C-T

47995959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97894614-T-C

47996028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97894666-T-C

47996028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97894666-T-G

47996031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97894684-G-A

47996031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97894684-G-T

47996036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97894689-A-G

47996040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97894693-G-A

47996040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97894693-G-T

47996402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97895055-T-C

47996402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97895055-T-G

47996403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97895056-G-A

47996403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97895056-G-T

47996409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97895059-G-A

47996409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97895059-G-T

47996520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97895170-G-A

47996520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97895170-G-T

47996536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97895186-G-A

47996536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97895186-G-C

47996572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: synonymous variant
orthologous variants: 97895217-C-T

47996614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 97895259-G-C

47997029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97895618-A-G

47997317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97895904-C-G

47997317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97895904-C-T

47997495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97896070-A-G

47997495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97896070-A-T

http://identifiers.org/hco/12/GRCh38#47997500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97896075-C-A

47997500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97896075-C-T

47997590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97896164-A-G

http://identifiers.org/hco/12/GRCh38#47997945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97896500-A-C

47997947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97896502-G-T

47998178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97896744-G-A

47998178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97896744-G-T

47998243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97896809-A-G

47998243-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97896809-A-T

47998255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97896821-G-A

47998337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97896892-A-G

http://identifiers.org/hco/12/GRCh38#47998347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97896902-C-A

47998347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97896902-C-G

47998351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97896906-G-A

47998351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97896906-G-T

47998363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97896923-G-C

47998363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97896923-G-T

47998369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97896929-A-G

47998477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97897210-A-T

47998516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97897242-G-A

47998516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97897242-G-T

47998588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97897311-G-A

47998674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97897395-G-A

47998674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97897395-G-T

47998725-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97897446-A-T

47999164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97897811-A-G

47999166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97897813-C-T

http://identifiers.org/hco/12/GRCh38#47999197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97897845-A-C

47999655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97898028-T-A

47999655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97898028-T-C

47999655-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97898028-T-G

http://identifiers.org/hco/12/GRCh38#47999666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97898039-C-A

47999666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97898039-C-G

47999666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97898039-C-T

47999752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97898110-G-A

47999752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97898110-G-C

47999752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97898110-G-T

47999768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97898129-G-A

47999768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97898129-G-T

47999977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97898342-A-T

48000156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97898516-G-A

48000156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97898516-G-T

48000220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97898577-A-G

48000231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97898592-G-A

48000231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97898592-G-T

48000247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97898610-T-C

48000247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97898610-T-G

http://identifiers.org/hco/12/GRCh38#48000256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97898627-C-A

48000272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97898643-T-C

48000386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97898762-G-C

48000449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97898819-G-A

http://identifiers.org/hco/12/GRCh38#48000851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97899082-C-A

http://identifiers.org/hco/12/GRCh38#48001275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97899452-C-A

48001398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97899583-G-A

48001532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97899727-G-C

http://identifiers.org/hco/12/GRCh38#48001617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97899809-C-A

48001640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97899832-C-T

48001651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97899843-T-A

48001904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97900100-T-C

http://identifiers.org/hco/12/GRCh38#48002223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97900447-C-A

http://identifiers.org/hco/12/GRCh38#48002295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97900521-C-A

http://identifiers.org/hco/12/GRCh38#48002538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97900803-C-A

48002538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97900803-C-T

48002604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97900868-C-T

48002645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97900907-G-T

http://identifiers.org/hco/12/GRCh38#48002647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97900909-C-A

48002727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97900990-A-G

48002776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97901053-T-C

48002832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97901119-A-G

48002882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97901169-G-A

48002882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97901169-G-T

48002911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97901208-C-T

http://identifiers.org/hco/12/GRCh38#48002931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97901228-C-A

48002931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97901228-C-T

48002962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97901259-G-A

http://identifiers.org/hco/12/GRCh38#48003328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97901601-C-A

48003328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97901601-C-G

48003328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97901601-C-T

48003454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97901664-G-A

48003538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97901727-G-A

48003660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97901836-G-A

http://identifiers.org/hco/12/GRCh38#48003866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97902014-C-A

48003866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97902014-C-T

48003928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97902044-G-C

48004006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97902095-T-C

48004006-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97902095-T-G

48004062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97902151-G-T

48004073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97902162-T-C

48004137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97902208-G-A

48004137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97902208-G-T

48004177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97902234-G-A

http://identifiers.org/hco/12/GRCh38#48004257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97902310-C-A

48004257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97902310-C-G

48004257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97902310-C-T

http://identifiers.org/hco/12/GRCh38#48004364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97902417-C-A

48004384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97902436-G-A

48004384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97902436-G-T

http://identifiers.org/hco/12/GRCh38#48004486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97902535-C-A

48004486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97902535-C-G

48004486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97902535-C-T

http://identifiers.org/hco/12/GRCh38#48004487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97902536-C-A

48004487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97902536-C-T

http://identifiers.org/hco/12/GRCh38#48004503-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97902552-A-C

48004503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97902552-A-G

48004503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97902552-A-T

http://identifiers.org/hco/12/GRCh38#48004537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97902586-C-A

48004537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97902586-C-T

48004561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97902611-G-A

48004561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97902611-G-C

48004561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97902611-G-T

48004638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97902687-G-A

48004638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97902687-G-T

http://identifiers.org/hco/12/GRCh38#48004684-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97902725-A-C

48004684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97902725-A-G

48004956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron variant
orthologous variants: 97902989-G-A

48005290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97903291-G-A

48005462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97903430-G-A

http://identifiers.org/hco/12/GRCh38#48005697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97903693-C-A

48005772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97903770-C-T

48005827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97903822-C-T