158731119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 3 prime UTR variant
orthologous variants: 116336576-G-A

158731119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 3 prime UTR variant
orthologous variants: 116336576-G-C

158731185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 3 prime UTR variant
orthologous variants: 116336533-G-A

158731185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 3 prime UTR variant
orthologous variants: 116336533-G-C

158731185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 3 prime UTR variant
orthologous variants: 116336533-G-T

158731670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 3 prime UTR variant
orthologous variants: 116336368-A-G

158731914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 3 prime UTR variant
orthologous variants: 116336134-G-A

158731914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 3 prime UTR variant
orthologous variants: 116336134-G-C

158732098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 3 prime UTR variant
orthologous variants: 116335947-T-A

158732098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 3 prime UTR variant
orthologous variants: 116335947-T-C

158732104-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 3 prime UTR variant
orthologous variants: 116335941-A-T

158732484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 3 prime UTR variant
orthologous variants: 116335568-T-C

158732484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 3 prime UTR variant
orthologous variants: 116335568-T-G

158732512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 3 prime UTR variant
orthologous variants: 116335540-G-A

158732600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 3 prime UTR variant
orthologous variants: 116335462-G-A

158732652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 3 prime UTR variant
orthologous variants: 116335442-T-C

158732921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 3 prime UTR variant
orthologous variants: 116335194-G-A

158732921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 3 prime UTR variant
orthologous variants: 116335194-G-T

http://identifiers.org/hco/7/GRCh38#158732939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116335176-C-A

158732970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 3 prime UTR variant
orthologous variants: 116335146-T-C

158733186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 3 prime UTR variant
orthologous variants: 116334945-T-C

158733288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 3 prime UTR variant
orthologous variants: 116334841-T-C

158733676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116334345-T-C

158733890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116334134-T-A

158733890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116334134-T-C

158733954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116334072-C-T

158734270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116333776-A-T

158734458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116333643-A-G

158734459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116333642-G-A

158734459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116333642-G-C

http://identifiers.org/hco/7/GRCh38#158735365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116332579-C-A

158735365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116332579-C-G

158735365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116332579-C-T

http://identifiers.org/hco/7/GRCh38#158735406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116332537-C-A

http://identifiers.org/hco/7/GRCh38#158736335-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116332146-A-C

http://identifiers.org/hco/7/GRCh38#158736558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116331962-A-C

158736752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116331805-C-T

158736833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116331647-C-T

158736977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116331530-C-G

158737015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116331491-G-A

http://identifiers.org/hco/7/GRCh38#158737459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116331066-A-C

158741070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116329983-C-T

158741254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116329767-T-C

158741403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116329616-A-G

158741418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116329601-A-G

http://identifiers.org/hco/7/GRCh38#158741502-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116329567-A-C

158741692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116329377-G-A

158742507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116328719-T-A

158742585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116328642-A-T

158742805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116328453-A-G

158743055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116327551-C-T

158743474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116327182-T-C

http://identifiers.org/hco/7/GRCh38#158744384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116326279-C-A

158744384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116326279-C-T

158748135-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116321610-T-A

158748172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116321576-T-C

158748186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 116321562-T-A

158748186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 116321562-T-C

158748198-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: missense variant
orthologous variants: 116321548-A-T

158748214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: missense variant
orthologous variants: 116321532-G-A

158748214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: missense variant
orthologous variants: 116321532-G-C

158748214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: missense variant
orthologous variants: 116321532-G-T

158748313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116321432-A-G

158749934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116320447-G-C

158749998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116320264-T-C

158750151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116320131-G-A

http://identifiers.org/hco/7/GRCh38#158750198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116320083-C-A

158750310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116319974-G-A

158750766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116319557-G-A

158750797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116319529-T-C

158751139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116319226-T-C

158751157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116319208-T-G

158751207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116319167-T-A

158751730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116318611-T-C

http://identifiers.org/hco/7/GRCh38#158752352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116317915-C-A

158752352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116317915-C-G

158752409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116317856-G-A

158752485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116317782-T-C

http://identifiers.org/hco/7/GRCh38#158752653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116317636-C-A

158752662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116317627-T-C

158752695-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116317595-A-T

158753055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116317265-A-G

158753164-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116317169-T-G

158753172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116317161-C-T

158753756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116316576-A-T

158754664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116315777-A-G

158757037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 116314138-G-A

158758197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116312897-C-G

158759005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116312279-C-T

158759103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116312183-G-A

158759462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116311956-A-G

158759498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: synonymous variant
orthologous variants: 116311920-T-C

158759535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: missense variant
orthologous variants: 116311883-A-G

158759538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: missense variant
orthologous variants: 116311880-C-T

158759542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: missense variant
orthologous variants: 116311876-C-T

http://identifiers.org/hco/7/GRCh38#158759596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116311822-A-C

http://identifiers.org/hco/7/GRCh38#158759611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116311808-C-A

158759611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116311808-C-T

158759614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116311805-T-C

158759906-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116311569-T-A

158759932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116311551-T-C

158760020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116311462-G-A

158760020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116311462-G-C

158760020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116311462-G-T

158760165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116311328-T-C

158760277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116311216-G-C

158760277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116311216-G-T

http://identifiers.org/hco/7/GRCh38#158760287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116311205-C-A

158760808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116310868-T-A

158760808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116310868-T-G

158760962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116310688-A-G

158761212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116310433-G-A

158761401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116310266-T-C

158761415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116310250-G-A

158761415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116310250-G-C

158761415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116310250-G-T

158761448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116310215-G-A

158761448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116310215-G-T

158762758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116307399-C-T

158762981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116307218-A-T

158762994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116307206-A-G

158762994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116307206-A-T

158763019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116307173-T-C

158763036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116307164-G-T

158763076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 116307145-T-C

158763850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116306697-G-A

158763941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116306624-G-A

158764312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116306196-A-G

158764461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116306068-T-G

http://identifiers.org/hco/7/GRCh38#158764526-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116306003-A-C

158764526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116306003-A-G

158764579-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116305955-A-T

158764620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116305914-C-T

http://identifiers.org/hco/7/GRCh38#158765202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116305460-C-A

158765216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116305446-T-C

158765255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116305397-T-C

158765309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116305344-T-C

158765413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116305256-T-C

158766543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116304821-A-G

158766573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116304791-T-G

158766717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116304513-T-C

158767546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116303387-G-A

158767546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116303387-G-T

158767585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116303342-T-C

158767585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116303342-T-G

158767736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: missense variant
orthologous variants: 116303203-T-C

158767757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: missense variant
orthologous variants: 116303182-A-G

158767889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116303016-A-G

158768353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116302664-T-C

158768936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116302545-T-C

158769119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116302366-T-C

158769139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116302351-C-T

158771322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116299250-G-A

http://identifiers.org/hco/7/GRCh38#158771525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116299018-C-A

158771525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116299018-C-T

158771602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116298950-C-G

158771791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116298749-A-G

158771808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116298731-T-A

158772525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron variant
orthologous variants: 116298247-G-A

158773451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116297763-T-A

158773451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116297763-T-C

158773455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116297759-G-A

158773455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116297759-G-T

http://identifiers.org/hco/7/GRCh38#158773508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116297716-C-A

158773508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116297716-C-G

158773508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116297716-C-T

158773547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116297677-T-G

158774179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116296826-C-G

158774530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116296492-T-C

158774643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116295035-C-T

158774707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116294978-G-A

158774781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116294903-G-A

158774781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116294903-G-C

http://identifiers.org/hco/7/GRCh38#158774935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116294750-C-A

158778339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116294315-C-G

158778341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116294313-G-A

158778346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116294308-T-C

158778391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116294264-C-T

158778444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116294210-T-A

158778444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116294210-T-C

158782865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116292748-C-G

158782865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116292748-C-T

158782869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116292744-T-C

158782947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116292708-A-G

158783061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116292598-G-T

158783065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116292593-C-G

158783065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116292593-C-T

158783420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116292075-C-G

http://identifiers.org/hco/7/GRCh38#158783428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116292067-A-C

158783609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116291844-G-A

158783760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116291699-C-T

158783785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116291668-T-G

158783803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116291650-G-A

158783803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116291650-G-C

158783811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116291642-T-C

158784052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116291497-G-C

http://identifiers.org/hco/7/GRCh38#158784199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116291381-A-C

158784247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116291339-A-G

158784385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116291230-C-T

158784389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116291226-G-T

158784459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116291154-G-A

158784759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116290912-A-G

158785298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116290611-G-A

158785328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116290583-G-A

158786095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116289935-T-C

158786257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116289770-C-G

158786709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116289412-C-T

http://identifiers.org/hco/7/GRCh38#158786879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116289238-C-A

158787120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116288867-G-A

158787513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116288392-T-C

158787694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116288213-T-C

http://identifiers.org/hco/7/GRCh38#158787927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116287904-C-A

http://identifiers.org/hco/7/GRCh38#158788339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116287536-A-C

158788339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116287536-A-T

158788419-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 116287456-T-A

158788474-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116287398-T-A

http://identifiers.org/hco/7/GRCh38#158788541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116287322-A-C

158793025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116285725-T-C

158793852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116284633-C-T

158798125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116282371-G-T

158798157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116282337-A-G

158798157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116282337-A-T

http://identifiers.org/hco/7/GRCh38#158798168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116282322-C-A

http://identifiers.org/hco/7/GRCh38#158798739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116281770-A-C

158799094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116281425-A-G

158799737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116280846-T-A

158806236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116275606-A-G

158806590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116275167-A-G

158806835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116274940-C-T

158806888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116274891-G-A

158811311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116270505-A-G

158811552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116270318-C-T

158811557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116270260-G-A

158811575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116270242-G-A

158811575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116270242-G-C

158811575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116270242-G-T

158811680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116270129-A-G

158811787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116270031-C-T

158811811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116270007-C-G

158818474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116258047-T-C

http://identifiers.org/hco/7/GRCh38#158819201-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#116257480-A-C

158819425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116257111-C-T

158819489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116257054-T-C

http://identifiers.org/hco/7/GRCh38#158821176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116251380-A-C

158821179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116251377-C-T

158821585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116250978-T-C

158821988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116248576-C-T

http://identifiers.org/hco/7/GRCh38#158824542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116247823-A-C

158824542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116247823-A-G

158824542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116247823-A-T

http://identifiers.org/hco/7/GRCh38#158825720-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116247437-A-C

158825720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116247437-A-G

158827389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116246844-T-C

158827524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116246732-G-T

158827530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116246726-C-T

http://identifiers.org/hco/7/GRCh38#158827714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116246522-C-A

158827714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116246522-C-G

http://identifiers.org/hco/7/GRCh38#158827959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116246260-A-C

158828114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116246113-T-C

158828502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116245798-G-A

http://identifiers.org/hco/7/GRCh38#158828601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116245701-C-A

158828602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116245700-C-G

158828698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116245620-G-A

158828735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116245589-G-A

158828735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116245589-G-C

158828768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116245555-G-A

158828797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116245527-G-C

158828797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116245527-G-T

http://identifiers.org/hco/7/GRCh38#158828811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116245513-A-C

158829011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116245350-G-A

158829011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116245350-G-T

158829016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116245345-G-A

158829016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116245345-G-C

http://identifiers.org/hco/7/GRCh38#158829119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#116245260-C-A

158829119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 116245260-C-T

http://identifiers.org/hco/7/GRCh38#158829167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#116245212-C-A

158829167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 116245212-C-T

158829334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 116245045-G-A

158829334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 116245045-G-T

http://identifiers.org/hco/7/GRCh38#158829350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#116245029-C-A

158829350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 116245029-C-G

158829418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, start_lost
orthologous variants: 116244961-T-A

158829418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22211
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, start_lost
orthologous variants: 116244961-T-C