http://identifiers.org/hco/12/GRCh38#120127330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115760659-C-A

120127332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: 3 prime UTR variant
orthologous variants: 115760655-C-G

120127359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: 3 prime UTR variant
orthologous variants: 115760628-T-C

120127359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: 3 prime UTR variant
orthologous variants: 115760628-T-G

120127468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: 3 prime UTR variant
orthologous variants: 115760542-C-T

120127469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: 3 prime UTR variant
orthologous variants: 115760541-G-A

120127469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: 3 prime UTR variant
orthologous variants: 115760541-G-T

http://identifiers.org/hco/12/GRCh38#120127606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115760457-C-A

120127606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: 3 prime UTR variant
orthologous variants: 115760457-C-T

120127609-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: 3 prime UTR variant
orthologous variants: 115760454-T-G

120127651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: 3 prime UTR variant
orthologous variants: 115760412-A-G

120128068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115760014-G-A

120128068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115760014-G-T

http://identifiers.org/hco/12/GRCh38#120128096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115759992-C-A

120128096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115759992-C-T

http://identifiers.org/hco/12/GRCh38#120128102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115759986-A-C

120128102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115759986-A-G

120128115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115759973-G-A

http://identifiers.org/hco/12/GRCh38#120129265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115759787-C-A

120129316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115759736-A-G

120129416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115759636-G-A

120129416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115759636-G-C

120129416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115759636-G-T

120129768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115759286-C-G

120129846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115759247-G-A

120129846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115759247-G-C

120129927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115759146-C-G

120130043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115758987-A-T

120130053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115758977-A-G

120130062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115758968-C-T

120130149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115758905-C-T

http://identifiers.org/hco/12/GRCh38#120130600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115758362-A-C

120130617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115758347-G-T

120130635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115758319-C-T

120130636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115758318-C-T

120130740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115758214-A-G

120130793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115758158-C-G

120130796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115758155-T-C

120130796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115758155-T-G

120130797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115758154-T-C

120130797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115758154-T-G

120130838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115758133-G-A

120130838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115758133-G-T

http://identifiers.org/hco/12/GRCh38#120130850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115758125-C-A

120130850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115758125-C-T

http://identifiers.org/hco/12/GRCh38#120130905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115758077-C-A

120130905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115758077-C-G

120130905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115758077-C-T

120130928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115758064-T-C

120131020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115757986-C-T

http://identifiers.org/hco/12/GRCh38#120131114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115757913-C-A

120131114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115757913-C-T

http://identifiers.org/hco/12/GRCh38#120131116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115757911-C-A

120131116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115757911-C-T

120131139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115757891-T-C

120131145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115757885-A-T

120131147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115757883-G-T

120131194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: synonymous variant
orthologous variants: 115757848-C-G

120131194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: synonymous variant
orthologous variants: 115757848-C-T

120131204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115757838-C-G

120131276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115757766-A-G

http://identifiers.org/hco/12/GRCh38#120131377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115757680-A-C

120131377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115757680-A-G

http://identifiers.org/hco/12/GRCh38#120131475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115757654-C-A

120131475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115757654-C-T

120131845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115757503-G-A

120131845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115757503-G-T

120131858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115757490-T-C

http://identifiers.org/hco/12/GRCh38#120131947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115757429-C-A

120131947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115757429-C-T

120132136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115757259-C-T

120132189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115757248-C-T

http://identifiers.org/hco/12/GRCh38#120132279-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115757195-A-C

120132488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115756970-T-C

120133418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115755203-G-C

120133439-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115755184-T-A

120134277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115754819-G-T

120134337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115754759-C-T

120134520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115754614-G-A

120134520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115754614-G-C

120134552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115754582-T-C

120134552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115754582-T-G

120134763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115754367-G-A

120134763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115754367-G-C

120134763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115754367-G-T

120136460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115753707-G-A

120136460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115753707-G-T

120136812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115753365-G-A

120136812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115753365-G-T

http://identifiers.org/hco/12/GRCh38#120136827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115753350-C-A

120136827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115753350-C-G

http://identifiers.org/hco/12/GRCh38#120136835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115753342-C-A

120136835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115753342-C-G

120137032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115753169-C-T

120137079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115753128-G-T

http://identifiers.org/hco/12/GRCh38#120137130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115753118-C-A

120137130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115753118-C-G

120137130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115753118-C-T

http://identifiers.org/hco/12/GRCh38#120137131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115753117-C-A

120137131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115753117-C-T

120137147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115753103-G-A

120137147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115753103-G-T

http://identifiers.org/hco/12/GRCh38#120137299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115752938-C-A

120137299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115752938-C-G

http://identifiers.org/hco/12/GRCh38#120137475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115752788-A-C

120137475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115752788-A-G

120137495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115752769-T-C

120137621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115752581-C-T

120137854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115752342-T-C

120137895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115752282-C-G

120137895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115752282-C-T

120137986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115752191-T-C

120138034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115752143-G-A

120138062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115752113-A-G

120138071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115752104-G-A

120138427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115751769-G-A

120138427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115751769-G-T

http://identifiers.org/hco/12/GRCh38#120138492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115751716-C-A

http://identifiers.org/hco/12/GRCh38#120138502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115751706-C-A

120138502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115751706-C-G

120138502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115751706-C-T

http://identifiers.org/hco/12/GRCh38#120138597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115751643-C-A

120138597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115751643-C-T

120138673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115751596-G-A

120138673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115751596-G-T

http://identifiers.org/hco/12/GRCh38#120138705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115751564-A-C

120138840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115751429-T-C

120140813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115750833-G-A

120140813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115750833-G-T

120140995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115750673-A-G

http://identifiers.org/hco/12/GRCh38#120141127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115750440-A-C

120141138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115750372-T-A

120141138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115750372-T-C

http://identifiers.org/hco/12/GRCh38#120141150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115750337-A-C

120141150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115750337-A-G

120141297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115750089-G-A

120141305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115750081-A-G

120141320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115750063-T-C

120141583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115749790-G-A

120141884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115749534-G-A

http://identifiers.org/hco/12/GRCh38#120141975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115749463-C-A

120141975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115749463-C-T

120142364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115749422-G-A

120142364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115749422-G-T

120142801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115749009-G-A

120142801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115749009-G-T

120143015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115748796-G-T

http://identifiers.org/hco/12/GRCh38#120144727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115747856-C-A

120144879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115747704-T-A

120144914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115747670-T-C

120144931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115747653-G-A

120145069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 115747515-G-A

120145147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115747447-G-A

120145147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115747447-G-C

120145275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115747341-T-C

120145281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115747335-A-G

120145344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115747271-G-A

120145344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115747271-G-T

120145345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115747270-G-A

120145345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115747270-G-T

120146417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115745217-T-C

120148117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115743096-T-C

120148121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115743092-G-A

120148121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115743092-G-T

120148217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115743004-T-C

120148292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115742929-G-C

120148361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115742860-C-T

http://identifiers.org/hco/12/GRCh38#120148436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115742788-C-A

120148436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115742788-C-T

120149571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115742202-G-A

120149748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115742039-G-C

http://identifiers.org/hco/12/GRCh38#120149776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115742012-C-A

120149776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115742012-C-T

120149786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115742002-G-C

http://identifiers.org/hco/12/GRCh38#120149926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115741387-C-A

120149926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115741387-C-T

120149986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115741327-T-C

120150109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115741236-A-G

120150156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115741193-A-G

120150172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115741184-C-T

120151099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115740733-G-A

120151099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115740733-G-T

120151104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115740728-A-G

120151258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115740576-T-A

120151258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115740576-T-C

120151345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115740489-A-G

120153139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115737389-T-C

120153139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115737389-T-G

http://identifiers.org/hco/12/GRCh38#120153173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115737358-C-A

120153173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115737358-C-T

120153189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115737342-G-A

120153189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115737342-G-T

120153238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115737298-G-A

120153256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115737280-A-G

120153334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115737202-G-A

120153358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115737178-G-A

http://identifiers.org/hco/12/GRCh38#120153366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115737170-C-A

120153366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: synonymous variant
orthologous variants: 115737170-C-T

120153495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115737087-G-C

120153495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115737087-G-T

120153716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115736948-G-A

http://identifiers.org/hco/12/GRCh38#120153725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115736939-C-A

120153725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115736939-C-T

120153757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115736910-T-C

120153775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115736892-G-A

120153799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115736868-T-C

120153968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115736709-G-A

120153968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115736709-G-T

http://identifiers.org/hco/12/GRCh38#120153971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115736706-C-A

120154034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115736661-G-C

120154085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115736611-C-T

120154478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115736271-G-C

120154846-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115735614-T-A

120154846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115735614-T-C

120154846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115735614-T-G

120154928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115735538-T-C

120155053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115735418-A-G

http://identifiers.org/hco/12/GRCh38#120155491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#115735060-C-A

120155491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115735060-C-G

120155491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115735060-C-T

120155712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115734920-A-G

120155729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115734904-G-A

120156209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115733714-G-A

120156211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115733712-G-A

120156223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115733700-G-T

120156320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115733611-G-C

120156320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115733611-G-T

120156386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115733551-A-G

http://identifiers.org/hco/12/GRCh38#120156396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115733541-C-A

120156449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115733505-C-G

120156486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115733468-G-A

120156486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115733468-G-C

120156489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115733465-C-T

120156504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115733450-G-C

120156507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115733447-C-G

120156507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115733447-C-T

120156617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115733337-T-C

http://identifiers.org/hco/12/GRCh38#120156688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115733282-C-A

120156688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115733282-C-T

120156705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115733266-A-G

120156705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115733266-A-T

120156886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115733156-C-G

120156886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115733156-C-T

http://identifiers.org/hco/12/GRCh38#120156903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115733139-C-A

120156903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115733139-C-G

120156905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 115733137-A-G

http://identifiers.org/hco/12/GRCh38#120156955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115733087-C-A

120156955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115733087-C-T

120156982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115733060-T-C

120157069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115733000-C-G

120157069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115733000-C-T

http://identifiers.org/hco/12/GRCh38#120157098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115732971-A-C

120157098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115732971-A-G

http://identifiers.org/hco/12/GRCh38#120157145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115732914-C-A

http://identifiers.org/hco/12/GRCh38#120157239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115732845-C-A

120157252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115732831-A-G

120157477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115732544-C-T

120157544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115732508-C-T

120157717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115732355-G-A

120157717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115732355-G-C

120157717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115732355-G-T

120157805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115732294-T-C

120158072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115732070-G-A

120158134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115732024-G-T

http://identifiers.org/hco/12/GRCh38#120158146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115732017-C-A

120158146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115732017-C-G

120158146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115732017-C-T

120158160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115732003-T-C

120158166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115731997-G-A

120158166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115731997-G-C

120158166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115731997-G-T

http://identifiers.org/hco/12/GRCh38#120158177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115731986-C-A

120158177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115731986-C-G

120158177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115731986-C-T

120158192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115731973-C-G

120158297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115731884-C-T

http://identifiers.org/hco/12/GRCh38#120158377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115731863-C-A

120158377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115731863-C-T

120158385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115731857-G-A

120158385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115731857-G-T

120158400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115731842-G-C

120158400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115731842-G-T

120158465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115731784-T-C

120158513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115731736-A-G

120158570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115731679-C-T

http://identifiers.org/hco/12/GRCh38#120158616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#115731633-C-A

120158649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115731604-A-G

120158649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115731604-A-T

120158670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115731583-A-G

120159522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115730908-C-G

120159674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115730706-A-T

120159684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115730697-T-C

http://identifiers.org/hco/12/GRCh38#120159694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115730687-C-A

120159694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115730687-C-T

120159753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115730631-C-G

120159839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115730550-C-T

120159926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115730463-G-C

120159926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115730463-G-T

120160001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115730388-G-A

120160001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115730388-G-C

120160051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115730339-G-A

120160051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115730339-G-T

120160100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115730290-G-A

120160100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115730290-G-T

120160117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115730261-G-A

120160117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115730261-G-T

120160130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115730247-G-A

120160130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115730247-G-T

http://identifiers.org/hco/12/GRCh38#120160275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115730103-C-A

120160275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115730103-C-T

120160308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115730071-T-C

120160357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115730024-A-G

120160733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115729709-T-C

120161121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115729383-G-A

120161354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115729225-G-A

120161354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115729225-G-T

120161428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115729163-G-T

120161450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115729146-G-T

120161542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115729072-T-C

120161603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115728996-C-T

120161658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115728700-A-G

120161731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115728631-A-G

120161788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115728572-T-C

120161903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 115728457-C-T

http://identifiers.org/hco/12/GRCh38#120162120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115728237-C-A

120162120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115728237-C-T

http://identifiers.org/hco/12/GRCh38#120162182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115728183-C-A

120162182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115728183-C-T

120162193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115728172-A-G

120162193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115728172-A-T

120162208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115728157-A-G

120162208-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115728157-A-T

http://identifiers.org/hco/12/GRCh38#120162239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115728126-C-A

120162239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115728126-C-T

120162262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115728104-G-T

120162265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115728101-G-A

120162265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115728101-G-T

120162266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115728100-T-C

120162326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115728052-T-C

120162371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115728006-A-G

120162371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115728006-A-T

120162374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115728003-G-A

120162374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115728003-G-C

120162374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115728003-G-T

http://identifiers.org/hco/12/GRCh38#120162375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115728002-A-C

120162375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115728002-A-G

120162375-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115728002-A-T

120162470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115727911-T-C

120162911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115727318-G-A

120163047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115727203-C-T

120163065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115727185-C-T

120163132-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115727118-T-A

120163288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115726959-C-T

120163512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115726803-A-G

120163644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115726707-G-A

120164222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115726285-T-C

120164229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115726278-G-A

120164229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115726278-G-T

120164382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115726146-G-A

120164397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115726131-C-G

120164432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: synonymous variant
orthologous variants: 115726096-A-G

120164508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115726020-G-A

120164508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115726020-G-T

120164627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115725950-G-A

120167603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115724637-T-C

120167971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115724287-G-A

120168022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115724230-C-T

http://identifiers.org/hco/12/GRCh38#120168067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115724183-C-A

120168098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115724155-G-A

120168098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115724155-G-T

120168167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115724039-T-C

http://identifiers.org/hco/12/GRCh38#120168191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115724015-A-C

120168191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115724015-A-G

120168207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 115723956-C-T

http://identifiers.org/hco/12/GRCh38#120168309-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115723854-A-C

120168334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115723829-C-T

120168362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115723803-T-A

120168362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115723803-T-C

120168372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115723793-A-G

120168372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115723793-A-T

120168375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115723790-T-A

120168489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115723674-G-T

120168609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115723570-C-T

http://identifiers.org/hco/12/GRCh38#120168727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115723470-C-A

120168826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115723412-T-G

120168947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115723285-C-T

120169916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115721837-T-C

120169989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115721739-C-G

120170100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115721651-G-T

120170150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115721626-G-A

120170155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115721621-C-T

120170177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115721599-G-A

120170216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115721560-G-A

120173679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115720468-A-G

http://identifiers.org/hco/12/GRCh38#120173772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115720375-C-A

120173772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115720375-C-T

120173873-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115720276-T-A

120173873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115720276-T-C

120173873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115720276-T-G

http://identifiers.org/hco/12/GRCh38#120173881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115720268-C-A

120173969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115720180-G-A

120173969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115720180-G-T

120173971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115720178-G-A

120173971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115720178-G-T

120173973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115720176-G-A

120173973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115720176-G-T

120173983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115720169-G-A

120173990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115720162-A-G

http://identifiers.org/hco/12/GRCh38#120174026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115719981-A-C

120174029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115719978-G-A

120174029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115719978-G-T

http://identifiers.org/hco/12/GRCh38#120174053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115719954-C-A

120174053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115719954-C-T

120174073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 115719934-T-C

120174076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115719931-T-C

120174076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115719931-T-G

http://identifiers.org/hco/12/GRCh38#120174170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#115719837-C-A

120175152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115719605-A-T

http://identifiers.org/hco/12/GRCh38#120175282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115719496-C-A

120175282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115719496-C-T

120175285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115719493-G-A

120175285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115719493-G-T

http://identifiers.org/hco/12/GRCh38#120175754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115719180-A-C

120175969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115718922-G-C

120176105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115718690-G-T

http://identifiers.org/hco/12/GRCh38#120177338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115718054-C-A

120177338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115718054-C-T

http://identifiers.org/hco/12/GRCh38#120177348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115718053-C-A

120177377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115718023-T-C

120177377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115718023-T-G

120177388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115718011-G-A

120177388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115718011-G-C

120177388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115718011-G-T

120177401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115717998-T-A

120177401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115717998-T-C

120177401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115717998-T-G

120177564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115717835-A-G

120177581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115717818-C-G

120177581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115717818-C-T

http://identifiers.org/hco/12/GRCh38#120177612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115717790-A-C

120177644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115717778-G-A

120177644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115717778-G-C

120177644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115717778-G-T

http://identifiers.org/hco/12/GRCh38#120178018-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115717620-A-C

120178458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115717374-A-G

120178543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115717330-G-C

120178543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115717330-G-T

http://identifiers.org/hco/12/GRCh38#120178550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115717323-C-A

120178564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115717317-C-T

120178567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115717314-G-A

120178567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115717314-G-T

120178583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115717308-C-T

120178644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115717248-T-A

http://identifiers.org/hco/12/GRCh38#120178790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115717103-A-C

120178812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115717086-T-C

http://identifiers.org/hco/12/GRCh38#120178830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115717063-C-A

120178830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115717063-C-G

120178830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115717063-C-T

120178895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115717004-G-A

120178910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense variant
orthologous variants: 115716989-C-G

120178954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 115716945-C-G

120178957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 115716942-G-C

120178975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115716925-G-A

120178975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115716925-G-C

120178975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115716925-G-T

120179015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115716886-T-C

120179015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115716886-T-G

120179059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115716853-T-C

http://identifiers.org/hco/12/GRCh38#120179060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115716852-C-A

120179061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115716851-T-C

http://identifiers.org/hco/12/GRCh38#120179096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115716823-C-A

120182311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, undefined
orthologous variants: 115715027-G-T

120182371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, undefined
orthologous variants: 115714977-C-G

120182420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, undefined
orthologous variants: 115714929-G-T

120182439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, undefined
orthologous variants: 115714903-G-A

120183033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115714686-C-T

120183211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115714524-G-A

120183212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115714523-A-G

http://identifiers.org/hco/12/GRCh38#120183418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115714386-C-A

120183418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115714386-C-T

http://identifiers.org/hco/12/GRCh38#120183431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115714374-C-A

120183502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115714350-G-A

120183502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115714350-G-T

120183690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115714164-G-T

120183708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115714142-G-A

120183708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115714142-G-T

120183719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115714126-C-T

120183722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115714118-C-T

120183757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115714077-G-A

120183757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115714077-G-C

120183757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115714077-G-T

120183762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115714069-G-A

120183762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115714069-G-T

120183966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115713550-G-T

120183968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115713548-T-C

120183978-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115713538-T-A

120183978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115713538-T-C

120183994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115713521-G-T

120184036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115713468-T-G

120184070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115713395-G-T

http://identifiers.org/hco/12/GRCh38#120184077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115713388-C-A

120184077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115713388-C-T

http://identifiers.org/hco/12/GRCh38#120184078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115713387-C-A

120184078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115713387-C-T

http://identifiers.org/hco/12/GRCh38#120184281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115713188-C-A

http://identifiers.org/hco/12/GRCh38#120184330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115713148-C-A

120184330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115713148-C-T

http://identifiers.org/hco/12/GRCh38#120184336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115713142-A-C

120184336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115713142-A-G

120184359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115713119-A-G

120184379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115713104-T-C

120184554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115712961-A-T

120184571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115712944-G-A

120184634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115712887-C-T

120184793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115712742-T-A

120184793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115712742-T-C

120184824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 115712699-C-T

http://identifiers.org/hco/12/GRCh38#120184977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115712553-C-A

120184977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115712553-C-T

120184983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115712547-G-T

http://identifiers.org/hco/12/GRCh38#120185005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115712516-C-A

120185005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115712516-C-T

120185164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115712382-G-A

120185277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115712288-C-T

120190403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 115709463-G-T

120190546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115709333-T-C

120190657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115709207-T-C

120191405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115707571-T-G

120191410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115707566-A-G

120191453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115707525-T-C

120191541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115707381-G-C

120191651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: 115707248-A-T

http://identifiers.org/hco/12/GRCh38#120194173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115703833-A-C

120194556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, undefined
orthologous variants: 115703488-G-C

120194556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, undefined
orthologous variants: 115703488-G-T

120194572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, undefined
orthologous variants: 115703472-G-A

120194572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4199
most severe consequence: intron_variant, undefined
orthologous variants: 115703472-G-T