http://identifiers.org/hco/1/GRCh38#200738976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136273779-C-A

200738976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 5 prime UTR variant
orthologous variants: 136273779-C-T

200739459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 5 prime UTR variant
orthologous variants: 136273445-C-T

200739466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 136273438-C-T

200739562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 136273382-G-A

200739562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 136273382-G-T

http://identifiers.org/hco/1/GRCh38#200739751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136273231-C-A

200739751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 5 prime UTR variant
orthologous variants: 136273231-C-G

200739751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 5 prime UTR variant
orthologous variants: 136273231-C-T

200739837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 136273164-G-A

200739837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 136273164-G-C

200739837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 136273164-G-T

200740030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136272976-T-C

200741345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136271845-T-C

200741621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136271645-T-G

200741877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136271417-T-C

200743134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136269976-C-T

200743273-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136269448-T-A

200743416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136269149-A-G

200744146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136268852-A-G

http://identifiers.org/hco/1/GRCh38#200746257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136267176-A-C

200746305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136267120-G-A

200746348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136267075-G-C

200748077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136263988-A-T

200748094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136263971-T-G

http://identifiers.org/hco/1/GRCh38#200748843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136262410-C-A

200748905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136262348-C-T

200748955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136262297-C-G

200748955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136262297-C-T

200749194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136262065-A-G

200749200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136262059-G-A

200749844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136261463-T-C

200753465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136259843-C-T

200753509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136259797-C-T

200754895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136258730-T-C

200755224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136258398-G-A

200755789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136257934-T-C

200758315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136254696-A-G

200758466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136254538-C-T

200758605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136254403-T-C

200758825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136253521-T-G

200758943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136253411-C-G

200760364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136253205-A-G

200761208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136252359-G-C

200761849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136251396-C-T

200761937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136251303-T-G

200762420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136250627-C-G

200762420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136250627-C-T

200762424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136250623-T-C

200762424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136250623-T-G

200762441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136250591-T-C

200762463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136250569-C-T

200762673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136250384-G-A

200764268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136249541-G-C

200764342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136249468-T-G

200768396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136245762-G-A

200768688-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136245514-T-A

200768702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136245509-G-A

200768942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136245455-T-C

200780933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136244042-A-G

200781337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136243678-G-A

200781337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136243678-G-T

200781368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136243648-A-G

200781389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136243627-T-C

200795390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136235575-T-C

200802923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron_variant, undefined
orthologous variants: 136234696-G-A

200803377-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136234133-G-C

200806521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136232958-A-G

200807114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136232423-A-G

200807542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136232026-G-T

200807545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 136232023-T-C

200807578-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136231994-A-T

http://identifiers.org/hco/1/GRCh38#200807608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136231965-C-A

200807608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136231965-C-T

200807976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136231788-C-T

200807997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136231776-C-T

200808243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136231528-T-C

200808397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136231252-C-G

200815462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136225618-C-T

200815464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136225616-G-A

200815464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136225616-G-T

http://identifiers.org/hco/1/GRCh38#200815619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136225503-C-A

200815619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: missense variant
orthologous variants: 136225503-C-T

200815652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 136225470-T-C

200827909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136225324-T-C

200828497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136225123-G-T

200828520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136225102-A-G

200828720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136224902-A-G

200828721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136224901-T-C

200828725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136224897-A-G

200829859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136223798-C-T

200829964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136223668-A-G

http://identifiers.org/hco/1/GRCh38#200829965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136223667-C-A

200830417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136223320-T-C

200830581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136223232-G-A

200830629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136223204-C-T

200830671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136223171-G-A

200830684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136223158-A-G

200830708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136223138-A-G

200830869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136222845-C-G

200831005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136222712-A-G

200831219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136222373-T-G

200831357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136222241-C-T

200831702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136221806-G-A

200831991-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136221524-A-T

200832161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136221187-G-T

200832272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136221085-G-A

200832290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136221067-G-C

200832333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136221024-G-C

200832353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136221004-A-G

http://identifiers.org/hco/1/GRCh38#200832365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136220993-C-A

http://identifiers.org/hco/1/GRCh38#200832446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136220958-C-A

http://identifiers.org/hco/1/GRCh38#200832638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136220811-A-C

200832638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136220811-A-G

200833644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136220197-T-C

200833644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136220197-T-G

200838118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136217788-A-G

200838118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136217788-A-T

200840117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136216857-C-T

200840125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136216849-C-T

200840645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136216660-T-C

200840948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136216362-C-T

200840991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136216310-G-A

200841125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136216206-C-T

200841845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136215894-A-G

http://identifiers.org/hco/1/GRCh38#200841857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136215882-C-A

http://identifiers.org/hco/1/GRCh38#200841887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136215855-C-A

200842166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136215493-T-G

http://identifiers.org/hco/1/GRCh38#200842176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136215434-C-A

200842186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136215359-T-A

200842186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136215359-T-C

http://identifiers.org/hco/1/GRCh38#200842213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136215311-C-A

200842213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136215311-C-G

200842221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136215298-A-G

200842295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136215214-T-C

200842315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136215193-T-G

200842351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136215147-G-A

200843726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136214101-G-A

200843823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136213998-G-A

200843823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136213998-G-C

http://identifiers.org/hco/1/GRCh38#200843826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136213995-C-A

200844805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 136213715-T-C

200844805-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 136213715-T-G

http://identifiers.org/hco/1/GRCh38#200844840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136213680-C-A

200846652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136212685-C-T

200847320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136211571-A-G

200847320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136211571-A-T

http://identifiers.org/hco/1/GRCh38#200847323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136211568-C-A

200847575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136210653-C-G

200847621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136210636-T-C

200847741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136210518-A-G

200847769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136210491-G-A

200847769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136210491-G-T

200847930-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136210331-T-A

200847930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136210331-T-C

200847992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136210273-T-A

200848084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 136210183-G-A

http://identifiers.org/hco/1/GRCh38#200848375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136209895-C-A

200848418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 136209852-A-G

http://identifiers.org/hco/1/GRCh38#200848672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136209598-A-C

200848804-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 136209466-T-G

200848819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 136209451-G-A

200848882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 136209388-A-T

200848937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 136209333-A-G

200849056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 136209214-G-A

http://identifiers.org/hco/1/GRCh38#200849161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136209109-A-C

200849161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 136209109-A-G

200849217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 136209053-T-C

200849248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 136209022-G-C

200849299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 136208971-C-T

200849346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 136208924-G-T

200849563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 136208707-G-A

200849605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 136208668-G-T

http://identifiers.org/hco/1/GRCh38#200849608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136208665-C-A

200849608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 136208665-C-G

200849641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 136208632-C-G

200849641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 136208632-C-T

200849667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 136208606-A-G

200850121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 136208155-T-C

http://identifiers.org/hco/1/GRCh38#200850314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136207976-C-A

200850314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136207976-C-T

200850654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136206709-A-G

200850791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136206614-G-A

200850881-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136206538-A-T

200851555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136206205-G-A

200851740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136206057-A-G

200851880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136205939-T-C

200852455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136205126-T-C

200852455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136205126-T-G

200852745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136204876-T-C

200852745-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136204876-T-G

200852791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136204825-G-A

200852791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136204825-G-T

200852849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 136204768-G-A

200853501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136204267-A-G

http://identifiers.org/hco/1/GRCh38#200853525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136204243-C-A

200853525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136204243-C-G

http://identifiers.org/hco/1/GRCh38#200853723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136204052-C-A

200853884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136203627-C-T

200854165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136203355-A-G

200854193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136203321-G-C

200854268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136203259-C-T

200854486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136202948-A-G

200854498-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136202936-T-A

200854498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136202936-T-C

200854577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136202835-C-T

http://identifiers.org/hco/1/GRCh38#200854696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136202729-C-A

http://identifiers.org/hco/1/GRCh38#200854705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136202720-C-A

200854705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136202720-C-T

200854734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136202692-T-C

200854910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136202516-T-C

200855337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136201951-G-C

200856186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136201421-G-A

200856235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136201381-A-G

200856259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136201306-G-T

200856277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136201288-A-T

200856362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136201223-C-T

200856463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136201054-T-C

200856581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136200898-T-C

200856720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136200777-G-C

200856836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136200642-C-T

200856878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136200346-C-T

200856888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136200336-A-G

200857187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136199602-G-A

200857187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136199602-G-T

200857193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136199596-G-A

200857193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136199596-G-C

200857193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron variant
orthologous variants: 136199596-G-T

200857432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 136199259-T-C

200857475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 136199213-A-G

http://identifiers.org/hco/1/GRCh38#200857489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136199185-A-C

http://identifiers.org/hco/1/GRCh38#200857504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136199170-C-A

200857594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 136199082-G-A

200857594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 136199082-G-C

200857691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 136198940-T-C

200857904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: missense variant
orthologous variants: 136198733-G-C

http://identifiers.org/hco/1/GRCh38#200858030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136198607-C-A

200858030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: missense variant
orthologous variants: 136198607-C-T

200858290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 3 prime UTR variant
orthologous variants: 136198350-G-C

200858290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 3 prime UTR variant
orthologous variants: 136198350-G-T

http://identifiers.org/hco/1/GRCh38#200858436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136198218-A-C

200858436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 3 prime UTR variant
orthologous variants: 136198218-A-G

200858542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 3 prime UTR variant
orthologous variants: 136198098-T-C

200858542-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 3 prime UTR variant
orthologous variants: 136198098-T-G

200858592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 3 prime UTR variant
orthologous variants: 136198048-G-T

200858626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 3 prime UTR variant
orthologous variants: 136198015-G-C

200858808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 3 prime UTR variant
orthologous variants: 136197840-G-T

200858867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 3 prime UTR variant
orthologous variants: 136197778-A-T

http://identifiers.org/hco/1/GRCh38#200858932-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136197709-A-C

200859973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 3 prime UTR variant
orthologous variants: 136196710-A-G

200860083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 3 prime UTR variant
orthologous variants: 136196600-T-C

200860318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 3 prime UTR variant
orthologous variants: 136196372-G-C

http://identifiers.org/hco/1/GRCh38#200860474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136196219-C-A

200860474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 3 prime UTR variant
orthologous variants: 136196219-C-T

200860674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29188
most severe consequence: 3 prime UTR variant
orthologous variants: 136196056-C-T