7329806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38190070-T-A

7329806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38190070-T-C

7329831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38190095-A-G

7329831-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38190095-A-T

7330044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38190294-G-A

7330097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38190381-A-G

7330249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38190476-A-G

7330565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38190729-A-G

7330588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38190752-C-T

http://identifiers.org/hco/6/GRCh38#7330736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38190878-C-A

7330925-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38191047-T-A

7330930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38191048-A-G

7333974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38191860-C-T

7333993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38191886-A-G

7334090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 38191984-A-G

7334090-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 38191984-A-T

7334118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38192011-G-T

7355040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, splice_donor_variant
orthologous variants: 38195323-C-T

7355058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 38195341-G-C

7355058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 38195341-G-T

http://identifiers.org/hco/6/GRCh38#7355204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38195493-C-A

7355217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38195509-T-A

http://identifiers.org/hco/6/GRCh38#7355229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38195521-C-A

7355229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38195521-C-G

7355229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38195521-C-T

7356218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38196551-A-G

http://identifiers.org/hco/6/GRCh38#7356229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38196562-C-A

7356257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38196590-T-C

7356366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38196693-C-T

7356444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38196771-T-A

http://identifiers.org/hco/6/GRCh38#7357142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38197603-A-C

7357143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38197604-G-A

7357175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38197635-A-G

7365114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38198677-G-C

7365346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38199537-T-C

7365383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38199578-T-C

7365383-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38199578-T-G

7365706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38200295-G-A

7365706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38200295-G-T

7365760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38200345-A-T

7365942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38200533-T-A

http://identifiers.org/hco/6/GRCh38#7368554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38201137-C-A

7368556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38201139-C-G

7368556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38201139-C-T

http://identifiers.org/hco/6/GRCh38#7368604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38201187-C-A

7368618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38201201-T-C

7368659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38201247-A-G

7368682-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38201267-T-A

7368682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38201267-T-C

7368778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 38201363-A-G

7368817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38201402-G-T

7368916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38201474-G-C

7368916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38201474-G-T

7368919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38201477-G-T

http://identifiers.org/hco/6/GRCh38#7369658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38202904-A-C

7369661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38202907-T-A

7369714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38202973-G-A

7369741-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38202996-A-T

7369742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38202997-G-A

7369809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38203039-T-C

7369809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38203039-T-G

http://identifiers.org/hco/6/GRCh38#7369820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38203050-C-A

7369820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38203050-C-G

7369820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38203050-C-T

http://identifiers.org/hco/6/GRCh38#7369823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38203053-C-A

7369823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38203053-C-T

7369845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38203081-A-T

http://identifiers.org/hco/6/GRCh38#7369868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38203107-C-A

7369868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38203107-C-T

7369927-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 38203151-T-G

7370008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 38203232-G-C

7370083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38203307-A-G

7370103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38203327-G-A

7370103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38203327-G-T

http://identifiers.org/hco/6/GRCh38#7370110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38203334-C-A

7370110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38203334-C-G

7372196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38205682-G-A

7372203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38205689-G-A

7372256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38205746-G-A

7372279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38205784-C-T

http://identifiers.org/hco/6/GRCh38#7372452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38206057-C-A

7372454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38206059-G-A

http://identifiers.org/hco/6/GRCh38#7372462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38206067-C-A

7372462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38206067-C-G

7372462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38206067-C-T

7372499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38206112-G-A

7372607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38206225-G-A

http://identifiers.org/hco/6/GRCh38#7372979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38206299-C-A

7372979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38206299-C-T

http://identifiers.org/hco/6/GRCh38#7372980-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38206300-A-C

7372980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38206300-A-G

7372992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38206311-G-A

7372992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38206311-G-C

7372992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38206311-G-T

7372993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38206312-T-C

7372994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38206313-G-T

http://identifiers.org/hco/6/GRCh38#7373001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38206320-C-A

7373001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38206320-C-T

7373006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38206325-T-A

7373006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38206325-T-C

7373006-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38206325-T-G

7373094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 38206410-G-A

7373449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 38206765-T-C

7373472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 38206788-T-C

7373968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 38207284-C-G

7373968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 38207284-C-T

7374108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38207421-T-A

http://identifiers.org/hco/6/GRCh38#7374164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38207477-C-A

7374164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38207477-C-G

7374164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38207477-C-T

7374434-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38207589-T-G

7376657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38208003-C-T

7376681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38208027-T-C

7376690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38208034-C-T

7376880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38208189-G-T

7376891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38208199-A-G

7377114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38208304-C-G

7377881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38208746-T-C

7377950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38208815-T-C

7377958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38208823-G-A

7378056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38208888-A-G

7378410-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38209137-T-A

http://identifiers.org/hco/6/GRCh38#7378518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38209250-C-A

7378518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38209250-C-T

7378556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38209288-G-A

7378556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38209288-G-T

7378582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38209314-T-C

7378680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38209412-C-T

7378731-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38209463-C-G

7378731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38209463-C-T

http://identifiers.org/hco/6/GRCh38#7378761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38209490-C-A

7378761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38209490-C-T

7378840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 38209569-T-C

7378863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38209592-C-T

http://identifiers.org/hco/6/GRCh38#7378869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38209598-A-C

7378902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38209664-A-G

7378902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 38209664-A-T

7378947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38209709-T-C

http://identifiers.org/hco/6/GRCh38#7379241-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38210080-A-C

7379764-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38210405-T-G

7380035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38210626-T-C

7380096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38210672-G-T

7380701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38211338-A-G

7380906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38211511-C-G

7380906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38211511-C-T

7380924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38211529-C-G

7385531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38211860-C-T

7385596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38211908-T-C

7385660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38211972-T-A

7385670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38211982-A-G

7385670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38211982-A-T

7385726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38212033-T-A

7385726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38212033-T-C

7385762-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38212057-A-T

7385827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38212121-G-T

7385828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38212122-T-C

7385836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38212130-C-T

http://identifiers.org/hco/6/GRCh38#7385987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38212280-A-C

7386012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38212305-G-C

7386012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38212305-G-T

7386127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38212398-G-A

7386168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38212438-T-C

7386210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38212964-T-C

7386428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38215773-C-T

7386454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38215796-T-A

7386505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38215845-G-C

7386535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38215878-C-T

7386565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38215909-G-A

7386641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38215996-C-T

http://identifiers.org/hco/6/GRCh38#7386668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38216038-C-A

7386668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38216038-C-G

7386679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38216054-C-T

7386808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38216166-A-G

7386833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38216191-G-A

http://identifiers.org/hco/6/GRCh38#7386855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38216225-C-A

7386895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38216264-A-G

7386895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38216264-A-T

7386965-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38216329-T-A

7386965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38216329-T-C

7387103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38216465-T-C

7387223-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38216641-T-A

7387227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38216651-T-A

7387227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38216651-T-C

7387578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38217113-G-T

7388994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38220266-A-T

7389161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38220686-G-A

7389311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 38220825-C-G

7389311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 38220825-C-T

7389456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 38220964-G-A

7389456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 38220964-G-T

7389593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 38221038-C-T

http://identifiers.org/hco/6/GRCh38#7389597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#38221042-C-A

7389597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 38221042-C-T

7389650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 38221093-C-G

7389661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 38221104-T-A

7389666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 38221109-G-A

7389666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 38221109-G-C

7389666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 38221109-G-T

7389718-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 38221165-T-A

7389718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 38221165-T-C

http://identifiers.org/hco/6/GRCh38#7389723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#38221169-C-A

7389723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21622
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 38221169-C-T