164894590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65141478-G-T

164895583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65143393-T-A

164895643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65143449-T-G

164895980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65143882-G-A

164896151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65144032-A-G

http://identifiers.org/hco/2/GRCh38#164896159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65144040-C-A

164896159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65144040-C-T

164896303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65144178-T-A

164896362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65144253-A-G

http://identifiers.org/hco/2/GRCh38#164896761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#65144663-C-A

164896780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65144672-G-T

164896791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65144681-T-C

164896835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65145363-G-A

http://identifiers.org/hco/2/GRCh38#164896949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#65145467-C-A

164896965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65145483-C-T

164897006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65145508-A-G

164897062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65145572-G-T

164897072-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65145582-T-A

164897076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65145586-C-G

164897076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65145586-C-T

164897356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65145801-G-A

164897376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65145823-C-T

164897440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65145854-G-T

164897480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65145898-G-A

164897480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65145898-G-T

http://identifiers.org/hco/2/GRCh38#164897597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65146266-C-A

164897597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65146266-C-G

164897671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65146355-G-A

164897675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65146359-T-C

164897765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65146402-G-T

164897788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65146424-T-C

164897804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65146440-C-T

164897828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65146463-T-C

164897837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65146474-T-A

164897862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65146499-G-C

164897862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65146499-G-T

164897863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65146500-T-C

http://identifiers.org/hco/2/GRCh38#164897882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65146519-C-A

164897882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65146519-C-T

164897896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65146532-T-C

http://identifiers.org/hco/2/GRCh38#164897907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65146543-C-A

164897938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65146574-A-G

164897961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65146597-A-G

http://identifiers.org/hco/2/GRCh38#164897963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65146599-C-A

http://identifiers.org/hco/2/GRCh38#164897987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65146623-C-A

http://identifiers.org/hco/2/GRCh38#164898012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65146646-C-A

164898012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65146646-C-G

164898012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65146646-C-T

164898025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65146659-T-C

http://identifiers.org/hco/2/GRCh38#164898060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65146669-C-A

164898060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65146669-C-G

164898060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65146669-C-T

http://identifiers.org/hco/2/GRCh38#164898080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65146693-A-C

164898080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65146693-A-G

164898080-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65146693-A-T

http://identifiers.org/hco/2/GRCh38#164898093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65146706-A-C

164898093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65146706-A-G

164898096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65146709-T-A

164898096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65146709-T-C

164898096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65146709-T-G

164898139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65146752-G-A

164898139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65146752-G-T

http://identifiers.org/hco/2/GRCh38#164898184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65146881-C-A

164898298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65146980-T-C

164898308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65146994-C-T

164898327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65147013-G-C

164898327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65147013-G-T

164898450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 65147094-C-G

164898450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 65147094-C-T

164898586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65147230-C-G

164898586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65147230-C-T

164898614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 65147258-A-G

164898668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 65147312-A-G

164898692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 65147336-T-G

164898695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 65147339-A-G

164898775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65147416-A-G

164898815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65147514-T-G

164898826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65147529-C-T

164898850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65147563-G-A

164898850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65147563-G-T

164898902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65147719-G-T

164899074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65148106-T-C

164899369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65148414-C-T

164899577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65148626-G-A

164899680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65148713-T-G

164899838-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65148866-T-G

164899873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65148897-C-T

164899953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65148983-G-T

164900105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65149212-T-C

164900167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65149279-A-T

164900190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65149296-C-T

164900373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65149467-C-T

164900386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65149480-A-G

http://identifiers.org/hco/2/GRCh38#164900398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65149490-C-A

164900467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65149537-T-C

164900605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65149659-A-G

http://identifiers.org/hco/2/GRCh38#164902725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65150049-C-A

164902790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65150106-A-G

http://identifiers.org/hco/2/GRCh38#164902803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65150160-C-A

164903941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65152741-T-C

164904104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65152903-C-T

164904176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65152965-C-G

164904316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65153143-A-G

164904666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65153489-G-C

164904674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65153497-T-C

164906221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65154927-T-C

164906454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65155205-C-T

164906578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65155328-C-T

164906639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65155436-G-A

164906689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65155488-G-A

164906985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65155777-G-A

164907085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65155880-G-A

164907113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65155907-C-T

164907114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65155908-T-C

164907213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65155965-A-G

164907254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65155978-C-T

164907675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65156128-T-C

164907697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65156149-T-C

164907836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65156295-G-A

164908065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65156471-G-T

http://identifiers.org/hco/2/GRCh38#164908499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65156730-A-C

http://identifiers.org/hco/2/GRCh38#164908513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65156744-C-A

164908513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65156744-C-T

164908537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65156774-A-G

164908565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65156808-A-G

164908641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 65156871-T-C

http://identifiers.org/hco/2/GRCh38#164908654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65156884-C-A

164908654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65156884-C-T

164908671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65156901-A-G

164908708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65156938-T-C

164908708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65156938-T-G

164908760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65156990-A-T

164908801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65157031-G-A

http://identifiers.org/hco/2/GRCh38#164908875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65157087-A-C

http://identifiers.org/hco/2/GRCh38#164909107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65157311-C-A

164909322-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65157494-T-A

164909646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65158204-G-A

164909646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65158204-G-T

164909690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65158250-A-G

164909691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65158251-C-T

164909738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65158290-C-T

164910593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65159166-C-T

164910627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65159196-C-T

164910709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65159269-A-G

164910808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65159365-G-A

164910874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65159430-C-T

164911047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65159561-T-G

http://identifiers.org/hco/2/GRCh38#164911183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65159695-C-A

164911249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65159749-A-G

164911306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65159807-C-T

164911460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65159965-G-C

164911499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65160522-A-G

http://identifiers.org/hco/2/GRCh38#164911532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65160557-C-A

164911853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65160821-C-T

http://identifiers.org/hco/2/GRCh38#164911961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65160887-C-A

164912043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65160898-G-T

http://identifiers.org/hco/2/GRCh38#164912048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65160903-C-A

164912048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65160903-C-T

164912050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65160905-T-C

164912052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65160907-T-A

http://identifiers.org/hco/2/GRCh38#164912129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65160913-C-A

164912146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65160917-T-C

164912177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65160942-G-A

164912282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65161048-A-G

164912403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65161184-G-T

164912546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65161319-G-C

164912546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65161319-G-T

164912561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65161334-T-C

http://identifiers.org/hco/2/GRCh38#164912638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65161412-C-A

164912638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65161412-C-T

164912712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65161496-A-G

164912937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65161646-A-G

164912937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65161646-A-T

164913324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65161997-C-G

164913370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65162038-C-T

164913403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65162071-C-T

164913436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65162095-G-C

164913840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65163626-G-A

164914009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65163888-C-T

164914079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65163959-G-A

164914081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65163961-G-A

164914081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65163961-G-C

164914100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65163981-C-T

http://identifiers.org/hco/2/GRCh38#164914297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65164180-C-A

164914347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65164227-G-A

164914355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65164235-C-T

164914601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65164442-T-G

164914795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65164597-G-A

164914977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65164789-G-A

164914977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65164789-G-T

http://identifiers.org/hco/2/GRCh38#164914983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65164800-A-C

164914983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65164800-A-T

164915013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65164829-G-T

164915059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65164873-C-T

164915064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65164878-T-C

164915107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65164929-T-C

164915212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 65165034-A-G

164915272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 65165094-T-A

164915293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65165115-A-G

164915375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65165198-G-C

http://identifiers.org/hco/2/GRCh38#164915453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65165267-C-A

164915664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65165490-A-G

http://identifiers.org/hco/2/GRCh38#164915765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65165953-C-A

164915765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65165953-C-T

164915774-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65165962-T-A

164915774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65165962-T-C

http://identifiers.org/hco/2/GRCh38#164915781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65165969-C-A

http://identifiers.org/hco/2/GRCh38#164915784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65165972-C-A

http://identifiers.org/hco/2/GRCh38#164915802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65165989-C-A

164915802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65165989-C-T

164915803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65165990-T-C

164916041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65166218-A-G

164916081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65166258-A-G

164916421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65166912-G-A

http://identifiers.org/hco/2/GRCh38#164916432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65166923-A-C

http://identifiers.org/hco/2/GRCh38#164916689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65167282-A-C

164916881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65167596-T-C

164916958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65167672-A-T

164917007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65167721-T-C

164917141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65167870-G-T

164917466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65168176-A-G

164918158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65168662-A-G

164918158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65168662-A-T

164918449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65168912-C-T

164920372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65170901-A-G

164920372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65170901-A-T

164920656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65171288-A-G

164920679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65171311-C-T

164920691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65171321-A-T

164920742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65171374-C-T

164920780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65171412-A-G

164920903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65171537-T-G

164920942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65171576-A-G

164920948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65171582-G-T

164922186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65172454-G-T

http://identifiers.org/hco/2/GRCh38#164922200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65172468-C-A

164922200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65172468-C-T

164922215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65172483-T-C

http://identifiers.org/hco/2/GRCh38#164922227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65172495-C-A

164922227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65172495-C-T

http://identifiers.org/hco/2/GRCh38#164922253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65172521-C-A

164922253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65172521-C-T

164922269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65172537-G-A

164922269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65172537-G-T

http://identifiers.org/hco/2/GRCh38#164922279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65172547-C-A

http://identifiers.org/hco/2/GRCh38#164922368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65172631-C-A

164925960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65174537-A-G

164926208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65174758-G-A

164928523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65175157-G-T

164928681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65175315-T-C

164928729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65175359-T-C

164928859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65175467-C-G

164928971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65175676-C-G

164929017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65175785-T-A

164929017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65175785-T-G

164929273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65176192-T-C

164929293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65176215-G-A

164929293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65176215-G-C

http://identifiers.org/hco/2/GRCh38#164929494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65176407-C-A

164929614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65176520-G-C

164932988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65176807-C-G

164933206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65177030-A-G

164933262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65177075-A-G

164933262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65177075-A-T

164933311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65177133-A-G

164933970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65177791-G-T

164933976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65177797-A-G

164934354-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65178145-T-A

164934354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65178145-T-C

164934360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65178150-A-G

164935189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65178923-T-C

164935345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65179065-C-T

http://identifiers.org/hco/2/GRCh38#164936397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65179926-C-A

164936397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65179926-C-T

164936408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65179937-C-T

http://identifiers.org/hco/2/GRCh38#164937331-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65180366-A-C

164937331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65180366-A-G

164937823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65181764-T-C

164937878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65181828-G-A

164937892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65181842-G-A

164937892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65181842-G-C

164937892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65181842-G-T

164937896-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65181846-A-T

164937900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65181850-G-A

164937900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65181850-G-C

164937900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65181850-G-T

164937938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65181910-T-C

164938050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65182024-G-A

164938176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65182157-G-A

164938281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65182260-A-T

164938289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65182268-C-G

164938371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65182343-T-C

http://identifiers.org/hco/2/GRCh38#164938451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65182400-C-A

http://identifiers.org/hco/2/GRCh38#164938561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65182570-A-C

164938597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65182707-G-C

164938611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65182721-A-G

164938777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65182899-T-C

164938803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65182911-G-A

http://identifiers.org/hco/2/GRCh38#164939031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65183335-C-A

164939176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65183634-C-G

164939504-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 65184161-T-A

164939699-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65184350-T-A

164939699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65184350-T-C

164939699-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65184350-T-G

164939704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65184355-A-G

164939704-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65184355-A-T

http://identifiers.org/hco/2/GRCh38#164939705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65184356-C-A

164939705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65184356-C-G

164939705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65184356-C-T

http://identifiers.org/hco/2/GRCh38#164939719-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65184370-A-C

164944424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65185530-A-G

164944432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65185538-T-C

164944441-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65185547-T-A

164944441-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65185547-T-G

164944669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65185768-G-A

164944669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65185768-G-T

164944769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65185861-G-T

164944830-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65187227-A-T

164945085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65187490-T-C

164945102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65187526-T-A

164945384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65188182-C-T

http://identifiers.org/hco/2/GRCh38#164945490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65188287-C-A

164945513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65188311-G-T

164945518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65188316-T-C

164945552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65188353-T-C

164945678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 65188483-A-G

164945741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65188559-A-G

164945761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65188590-C-T

164945762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65188591-A-G

164945762-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65188591-A-T

164950797-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65189563-A-T

164950861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65189621-T-G

164951015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65189775-A-G

164951034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65189794-T-C

164951071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65189829-C-T

164951079-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65189837-A-T

164951102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65189845-T-C

164951175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65189918-C-T

164951769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65190589-G-A

164951809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65190663-C-G

164952374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65191353-A-G

164952582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65191554-G-A

164952582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65191554-G-C

http://identifiers.org/hco/2/GRCh38#164952594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65191566-C-A

164952594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65191566-C-T

http://identifiers.org/hco/2/GRCh38#164952806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65191770-C-A

164952827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65191790-T-A

164952827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65191790-T-C

164952843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65191809-C-T

http://identifiers.org/hco/2/GRCh38#164952866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65191825-A-C

164952904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65191855-G-A

164952904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65191855-G-T

164952915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65191867-A-G

164952915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65191867-A-T

164952949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65191907-A-T

164952972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65191930-T-A

http://identifiers.org/hco/2/GRCh38#164952999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65191957-C-A

164952999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65191957-C-G

164952999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65191957-C-T

164953081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65192039-A-T

http://identifiers.org/hco/2/GRCh38#164953141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65192091-C-A

164953141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 65192091-C-T

164953214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65192148-T-C

164953229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65192163-G-A

164953288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65192226-C-T

164953296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65192234-G-A

164953296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65192234-G-T

http://identifiers.org/hco/2/GRCh38#164953493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65192435-C-A

164953493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65192435-C-T

164953594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65192532-C-T

164953639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65192577-G-A

http://identifiers.org/hco/2/GRCh38#164953723-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65192663-A-C

164953723-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65192663-A-T

164953889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65193032-G-A

164953995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65193142-G-A

164953995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65193142-G-T

164954556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65193608-A-G

164954596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65193651-T-C

164954596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65193651-T-G

164954601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65193656-T-C

164954716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 65193776-A-G

164954718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 65193778-C-T

164954747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 65193818-T-A

http://identifiers.org/hco/2/GRCh38#164954762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65193833-C-A

164954762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65193833-C-G

164954762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65193833-C-T

164954895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65193938-A-G

164954950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65193986-C-G

164955053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65194120-A-G

164955132-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65194190-A-T

164955221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 65194237-G-T

164955233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 65194249-C-T

164955253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65194269-A-G

164955274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65194282-G-T

http://identifiers.org/hco/2/GRCh38#164955306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65194315-C-A

164955306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65194315-C-G

164955306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65194315-C-T

http://identifiers.org/hco/2/GRCh38#164955374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65194374-A-C

164955374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65194374-A-G

164955406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65194396-G-A

164955406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65194396-G-C

164955406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65194396-G-T

164955421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65194414-G-A

164955421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65194414-G-T

164955445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65194436-A-G