http://identifiers.org/hco/1/GRCh38#31790513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129850819-C-A

31790550-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129850806-G-C

http://identifiers.org/hco/1/GRCh38#31790559-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129850797-A-C

31790615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 129850741-A-G

31790616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129850740-G-T

http://identifiers.org/hco/1/GRCh38#31790654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129850703-C-A

31790654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 129850703-C-T

31790682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129850687-G-A

31790682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129850687-G-T

http://identifiers.org/hco/1/GRCh38#31790907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129850474-C-A

31790916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129850465-G-A

31791112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 129850302-A-G

31791162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129850252-C-T

31791178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129850236-A-T

31791196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129850218-G-T

31791359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129850023-T-C

31791399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129849999-A-T

31792039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129849488-G-A

31792039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129849488-G-T

http://identifiers.org/hco/1/GRCh38#31792070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129849458-C-A

31792070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129849458-C-T

http://identifiers.org/hco/1/GRCh38#31792304-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129849279-A-C

31792344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 129849239-G-C

31792672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129848777-A-T

http://identifiers.org/hco/1/GRCh38#31792748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129848700-C-A

31792748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129848700-C-T

31792773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 129848675-G-A

31792776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129848672-A-G

31792782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129848664-G-A

31792782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129848664-G-C

31792782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129848664-G-T

31792839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129848607-C-T

http://identifiers.org/hco/1/GRCh38#31792882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129848576-C-A

http://identifiers.org/hco/1/GRCh38#31792910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129848547-C-A

http://identifiers.org/hco/1/GRCh38#31793127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129848344-C-A

31793127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129848344-C-G

http://identifiers.org/hco/1/GRCh38#31793330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129848207-C-A

31793330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129848207-C-G

31793330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129848207-C-T

31793382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129848155-G-C

31793382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129848155-G-T

http://identifiers.org/hco/1/GRCh38#31793386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129848151-C-A

31793386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129848151-C-T

31793411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129848126-A-G

31793411-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129848126-A-T

http://identifiers.org/hco/1/GRCh38#31793465-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129848089-A-C

31793465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129848089-A-G

31793682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129847874-C-G

31793697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129847859-T-C

31793801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129847756-G-T

31793976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129847580-G-A

31793976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129847580-G-T

31794001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129847555-T-C

31794024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129847531-G-A

31794024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129847531-G-T

31794088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129847468-C-G

31794088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129847468-C-T

31794099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129847459-G-T

http://identifiers.org/hco/1/GRCh38#31794119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129847439-C-A

31794119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129847439-C-T

31794131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129847427-G-A

31794131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129847427-G-T

31794173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129847385-C-T

31794194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129847364-G-C

31794225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129847333-A-T

31794304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129847252-G-A

31794304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129847252-G-T

31794791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129846968-G-A

http://identifiers.org/hco/1/GRCh38#31795041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129846881-C-A

31795231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129846736-A-G

31795348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129846666-T-C

31795524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129846518-C-T

31795660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129846393-G-A

31795660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129846393-G-T

http://identifiers.org/hco/1/GRCh38#31795679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129846380-C-A

http://identifiers.org/hco/1/GRCh38#31795826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129846229-C-A

31795944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129846124-A-T

http://identifiers.org/hco/1/GRCh38#31796023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129846052-C-A

http://identifiers.org/hco/1/GRCh38#31796024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129846051-A-C

31796024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129846051-A-G

http://identifiers.org/hco/1/GRCh38#31796067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129846014-C-A

31796122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129845970-G-T

31796161-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 129845953-T-A

31796303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 129845842-T-C

31796303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 129845842-T-G

31796307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129845838-G-T

31796729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129845516-G-T

31796753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129845498-G-C

http://identifiers.org/hco/1/GRCh38#31796863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129845396-A-C

31796968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129845297-A-G

31797027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129845236-T-C

31797152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129845111-T-A

http://identifiers.org/hco/1/GRCh38#31797934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129843194-C-A

31797934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129843194-C-T

31798077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129843096-G-T

http://identifiers.org/hco/1/GRCh38#31798093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129843073-C-A

31798093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129843073-C-G

31798157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129843038-C-G

http://identifiers.org/hco/1/GRCh38#31798164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129843031-C-A

31798164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129843031-C-T

http://identifiers.org/hco/1/GRCh38#31798179-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129843019-A-C

31798255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129842950-C-T

http://identifiers.org/hco/1/GRCh38#31798271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129842934-C-A

31798271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129842934-C-T

31798326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 129842878-G-C

31798326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 129842878-G-T

31798344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129842863-G-C

31798369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129842842-C-T

31798415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129842812-C-T

31798711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 129842527-T-C

31798712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 129842526-G-T

http://identifiers.org/hco/1/GRCh38#31798730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129842510-C-A

http://identifiers.org/hco/1/GRCh38#31798753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#129842487-C-A

31798753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 129842487-C-T

31798849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129842366-G-T

31798879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129842346-T-A

31798879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129842346-T-C

http://identifiers.org/hco/1/GRCh38#31798880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#129842345-C-A

http://identifiers.org/hco/1/GRCh38#31798892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#129842333-C-A

31798892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129842333-C-G

31798896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129842329-T-A

31798899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129842326-C-G

31798899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129842326-C-T

31798974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129842248-G-A

31798974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129842248-G-C

31798974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129842248-G-T

31799105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129842094-T-C

31799273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129841668-A-G

31799495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129841452-G-T

31799505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129841442-C-G

31799505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129841442-C-T

31799538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129841409-G-A

31799538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129841409-G-T

http://identifiers.org/hco/1/GRCh38#31799801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129841304-C-A

31799838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129841267-T-C

31800025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129841127-T-C

31800027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129841125-C-G

31800027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129841125-C-T

31800093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129841056-G-A

31800097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129841052-A-G

31800109-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129841040-T-G

31800110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129841039-G-A

31800237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129840926-A-G

31800289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129840883-A-G

31800314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129840862-T-C

31800326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129840857-T-C

31800389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129840809-G-C

31800389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129840809-G-T

31800539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 129840666-C-G

31800539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 129840666-C-T

31800622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 129840598-G-A

31800622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 129840598-G-C

31800622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 129840598-G-T

http://identifiers.org/hco/1/GRCh38#31800716-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129840523-A-C

31800716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129840523-A-G

31800716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129840523-A-T

31800760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129840485-G-A

31800760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129840485-G-T

31800772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129840473-T-A

31800804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129840448-T-C

31800907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129840345-A-G

http://identifiers.org/hco/1/GRCh38#31800952-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129840308-A-C

31800953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129840307-C-T

31801126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129840200-C-T

31801512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129839867-A-G

31801695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129839705-T-C

31801722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129839676-A-T

http://identifiers.org/hco/1/GRCh38#31801748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129839650-C-A

31801748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129839650-C-T

31801754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129839640-C-T

31802353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129839406-G-A

31802353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129839406-G-T

31802407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129839356-G-C

31802514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129839263-A-G

31802797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129838977-G-A

31802797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129838977-G-C

31802798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129838976-C-T

31802896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129838880-G-T

31803204-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129838625-T-A

31803204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129838625-T-C

31803246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129838593-G-A

http://identifiers.org/hco/1/GRCh38#31809499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129830052-C-A

31809499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129830052-C-T

31809583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129829969-A-G

31809595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129829956-T-C

31809957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129829643-G-A

31810086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129829529-C-G

31810086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129829529-C-T

http://identifiers.org/hco/1/GRCh38#31810181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129829451-C-A

31810274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129829317-C-T

31810844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129828708-G-C

31810953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129828622-A-G

31811001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129828574-G-A

31811776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129828176-C-T

31811863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129828087-T-C

31812122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129827853-T-C

31812358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129827663-T-C

31812684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129825368-A-T

31812724-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129825335-T-G

31813026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129825110-T-C

31813097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129825029-C-T

http://identifiers.org/hco/1/GRCh38#31813705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129824444-A-C

31813773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129824377-G-A

31813818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129824208-G-T

31813838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129824170-A-G

31813857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129824143-C-T

31813863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129824137-G-C

31813863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129824137-G-T

31813908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129824035-A-G

31813938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129824007-A-G

31813972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129823973-G-A

http://identifiers.org/hco/1/GRCh38#31814350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129823676-C-A

31814350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 129823676-C-T

31814354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, missense_variant
orthologous variants: 129823672-G-A

31814354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, missense_variant
orthologous variants: 129823672-G-C

31814354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, missense_variant
orthologous variants: 129823672-G-T

31814376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, stop_gained
orthologous variants: 129823650-G-A

31814376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, missense_variant
orthologous variants: 129823650-G-C

31814376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, missense_variant
orthologous variants: 129823650-G-T

31814445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, missense_variant
orthologous variants: 129823581-G-T

31814467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 129823559-G-A

31814467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 129823559-G-C

31814467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 129823559-G-T

31814530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 129823499-A-G

31814530-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 129823499-A-T

31814546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, missense_variant
orthologous variants: 129823489-T-C

31814600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, missense_variant
orthologous variants: 129823435-T-C

31814678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, missense_variant
orthologous variants: 129823378-T-C

31814816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, missense_variant
orthologous variants: 129823258-C-T

31814853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, missense_variant
orthologous variants: 129823218-A-G

31814853-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, missense_variant
orthologous variants: 129823218-A-T

31814922-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 129823149-T-G

31814960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron_variant, missense_variant
orthologous variants: 129823111-T-C

31815345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 129823067-T-C

31815454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron variant
orthologous variants: 129822988-T-C

http://identifiers.org/hco/1/GRCh38#31815486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129822951-C-A

31815486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: intron variant
orthologous variants: 129822951-C-T

31815813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 129822690-T-C

31815813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 129822690-T-G

31815861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 129822657-G-C

31815861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 129822657-G-T

31815921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26338
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 129822626-A-G