90622270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15286477-T-C

90622362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15286374-G-T

http://identifiers.org/hco/8/GRCh38#90622556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15286175-C-A

90622628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15286117-C-T

90622884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15285888-G-A

90623002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15285783-T-C

90623100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15285738-A-G

90623270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15285600-T-G

90623441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15285435-A-G

90623738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15285145-T-C

http://identifiers.org/hco/8/GRCh38#90623773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15285110-C-A

90623773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15285110-C-G

90623811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15285072-C-T

http://identifiers.org/hco/8/GRCh38#90624175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15284806-C-A

90624175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15284806-C-G

90624248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15284731-C-T

http://identifiers.org/hco/8/GRCh38#90625273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15283727-A-C

90625289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15283711-C-G

90625331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15283679-C-T

90625917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15283106-A-G

90627337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15282968-T-C

90627463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15282852-T-A

90627463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15282852-T-G

90629551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15281649-T-G

90629594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15281608-T-C

90631426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15281258-G-A

90631426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15281258-G-T

90631520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15281194-A-T

http://identifiers.org/hco/8/GRCh38#90631521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15281193-A-C

http://identifiers.org/hco/8/GRCh38#90631540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15281172-C-A

90631540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15281172-C-T

90631649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 15281063-G-A

90631652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 15281060-G-T

http://identifiers.org/hco/8/GRCh38#90631658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15281054-A-C

90631658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 15281054-A-T

90631683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 15281029-A-G

90631696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 15281016-G-A

90631696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 15281016-G-C

http://identifiers.org/hco/8/GRCh38#90631708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#15281004-C-A

90631727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15280986-G-A

90631727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15280986-G-C

http://identifiers.org/hco/8/GRCh38#90631729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15280984-A-C

90631729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15280984-A-T

90631795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15280932-G-A

90631795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15280932-G-T

90632020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15280716-C-T

90632224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15280576-G-A

90632263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15280552-C-T

90633119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15280239-G-A

http://identifiers.org/hco/8/GRCh38#90633213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#15280144-A-C

90633213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15280144-A-G

90633763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15279685-T-A

90633763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15279685-T-C

http://identifiers.org/hco/8/GRCh38#90634891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15278764-C-A

90634990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15278677-T-C

90635087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15278586-A-G

90635171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15278515-C-T

90635552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15278234-A-T

90635567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15278219-T-C

90635571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15278215-G-C

90635612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15278179-G-A

90635612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15278179-G-T

http://identifiers.org/hco/8/GRCh38#90635805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15278051-A-C

90636600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15277186-T-C

http://identifiers.org/hco/8/GRCh38#90636665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15277149-C-A

90636730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15277093-T-C

90636750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15277078-G-C

90636848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15276971-G-A

90637331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15276476-C-T

90637398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15276415-T-C

90637511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15276297-G-C

90637867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15275251-T-C

http://identifiers.org/hco/8/GRCh38#90637922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15275199-C-A

90637952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15275170-T-A

90637952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15275170-T-C

90638031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15275101-A-T

90638039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15275089-C-T

90638523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15274693-G-A

90638857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15274408-C-T

90638963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15274299-A-T

90638987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15274275-T-A

90639061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15274202-T-A

90639145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15274135-C-T

90639270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15274019-A-G

90639298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15273994-T-G

http://identifiers.org/hco/8/GRCh38#90639791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15273553-A-C

90639826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15273520-A-G

90640068-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15273310-T-G

90640692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15272794-A-G

90640767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15272707-A-G

90641486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15272094-T-C

90641572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15272012-G-A

90641700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15271931-G-C

90641700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15271931-G-T

90641770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15271862-T-C

90641882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15271764-A-G

90642279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15269120-T-C

http://identifiers.org/hco/8/GRCh38#90642315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15269086-C-A

90642674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15268769-T-C

90643098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15268379-G-A

90643124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15268367-C-G

http://identifiers.org/hco/8/GRCh38#90643270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15268222-C-A

90643454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15268050-C-G

90643476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15268028-T-A

90643639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15267881-C-T

90643697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15267821-A-G

http://identifiers.org/hco/8/GRCh38#90643780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15267748-A-C

90644279-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15267450-G-C

90644332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15267420-A-G

90644356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15267392-T-G

http://identifiers.org/hco/8/GRCh38#90645001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#15266854-C-A

90645027-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15266840-T-A

90645027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15266840-T-C

90645136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 15266722-A-G

90645473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 15266385-G-A

90645473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 15266385-G-T

90645496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 15266362-A-G

http://identifiers.org/hco/8/GRCh38#90645568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15266290-C-A

90645568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 15266290-C-G

90645835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 15266020-A-G

90645896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 15265959-G-A

90645896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 15265959-G-T

http://identifiers.org/hco/8/GRCh38#90645924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15265943-C-A

90645924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15265943-C-T

90645997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15265867-A-G

http://identifiers.org/hco/8/GRCh38#90646012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15265852-C-A

90646012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15265852-C-T

90646020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15265844-A-T

90646059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15265809-G-C

90646059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15265809-G-T

90646066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15265802-G-A

90646066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15265802-G-C

90646066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15265802-G-T

http://identifiers.org/hco/8/GRCh38#90646073-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#15265795-A-C

90646073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15265795-A-G

http://identifiers.org/hco/8/GRCh38#90646093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15265775-C-A

http://identifiers.org/hco/8/GRCh38#90646103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15265765-C-A

90646103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15265765-C-G

90646103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15265765-C-T

90646158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15265726-G-A

90646158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15265726-G-T

90646227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15265657-G-A

90646517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 15265422-T-C

90646754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15265222-G-A

90646754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15265222-G-T

90648250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15265011-A-G

90648250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15265011-A-T

90648267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15264997-G-A

90648358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15264915-G-A

90648358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15264915-G-T

90648450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15264822-G-A

90648493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15264774-G-A

90648548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15264722-A-G

90648571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15264700-G-T

90648619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15264653-A-G

90648620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15264652-T-C

90648624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15264648-T-C

90648807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15264506-G-A

90649124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15264252-G-A

90649124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15264252-G-T

90649254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15264128-A-G

90649339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15264043-A-G

90649414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15263983-G-T

http://identifiers.org/hco/8/GRCh38#90649509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#15263899-C-A

90649509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 15263899-C-T

90649510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 15263898-T-A

90649510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 15263898-T-C

90649524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15263884-A-G

90649528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15263883-G-T

90649555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 15263857-T-C

90649582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15263830-T-G

90649583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15263829-G-T

90649613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15263799-A-G

90649722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15263690-G-T

http://identifiers.org/hco/8/GRCh38#90649815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15263605-C-A

http://identifiers.org/hco/8/GRCh38#90649835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15263585-C-A

90649835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15263585-C-T

90650005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15259173-G-A

90650027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15259155-G-A

90650027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15259155-G-T

http://identifiers.org/hco/8/GRCh38#90650072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15259110-C-A

90650072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15259110-C-T

90650120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15259065-G-A

90650120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15259065-G-T

90650156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15259034-T-C

90650331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15257327-A-T

90650334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15257324-G-A

90650334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15257324-G-C

90650369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15257289-C-T

90650398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15257258-C-T

90650525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15257124-A-G

90650979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15256942-G-A

90650979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15256942-G-T

90651009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15256915-C-T

90651021-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15256903-A-T

90651129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15256829-T-C

90651138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15256822-G-A

90651139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15256821-A-T

90651144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15256816-A-T

90651201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15256781-A-T

http://identifiers.org/hco/8/GRCh38#90651208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15256774-C-A

90651208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15256774-C-T

90651372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15256648-G-C

90651372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15256648-G-T

90651533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15256564-A-G

90651619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15256477-C-G

http://identifiers.org/hco/8/GRCh38#90651692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15256414-A-C

90652322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15256140-G-A

90652482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15255767-T-C

90652487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15255762-C-T

90652499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15255750-T-G

90652833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15254759-G-A

90652833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15254759-G-T

90652873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15254719-C-G

http://identifiers.org/hco/8/GRCh38#90652963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15254650-C-A

90652963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15254650-C-T

90653071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15254539-G-A

90653141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15254500-T-C

90653160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15254481-A-G

90653164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15254477-A-G

90653187-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15254453-A-T

90653364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15254294-T-C

90653453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15254211-T-C

90653506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15254158-C-T

90654386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15252825-C-G

90654424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15252793-A-G

90654648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15252574-G-T

90654662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15252560-A-G

http://identifiers.org/hco/8/GRCh38#90654726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15252497-A-C

http://identifiers.org/hco/8/GRCh38#90654764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15252463-C-A

90654764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15252463-C-T

90659250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15252134-C-T

90659419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15251967-G-A

90670988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15234390-G-A

90670988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15234390-G-C

90671025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15234354-A-G

90671783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15233667-G-A

90671806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15233644-T-C

90672928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15233477-A-G

90673386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15233101-A-G

90673677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15232122-C-T

90673799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15232013-G-A

http://identifiers.org/hco/8/GRCh38#90673823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15231990-C-A

90673982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15231840-T-C

90674433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15230042-T-C

90674564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15229939-C-T

90674765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15229744-C-T

http://identifiers.org/hco/8/GRCh38#90674780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15229730-C-A

90674871-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15229457-T-G

90674913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15229411-G-A

90675025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15229298-C-T

http://identifiers.org/hco/8/GRCh38#90675185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15229201-C-A

90675185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15229201-C-T

90675285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15229104-A-G

90675343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15229044-T-C

90675343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15229044-T-G

90675347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15229037-C-G

90675447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15228948-G-A

90675658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15228740-A-G

90676513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15227889-G-C

90676532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15227870-G-C

90676636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15227768-G-A

http://identifiers.org/hco/8/GRCh38#90677554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15218626-A-C

90677716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15218467-A-G

90678209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15217917-A-G

90690711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15215732-G-A

90690711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15215732-G-C

90691149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15215326-G-A

90691156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15215319-A-G

90691156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15215319-A-T

90691198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15215277-C-T

90691239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15215249-G-T

90691319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15215168-C-T

90691642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15214878-G-A

90691694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15214829-A-T

90692437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15214030-T-A

90692509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15213958-C-T

90692665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15213768-A-G

90692665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15213768-A-T

90692668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15213765-C-T

90692843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15213588-C-T

90692917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15213514-G-C

90692969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15213458-T-C

90692993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15213435-C-T

90693261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15213178-A-G

90694059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15211884-G-A

90694189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15211755-T-C

90694247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15211694-G-A

90694300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15211639-G-C

90694324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15211616-G-A

90694340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15211598-T-C

90694701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15211268-A-G

90694757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15211213-G-C

90694765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15211205-C-T

http://identifiers.org/hco/8/GRCh38#90695449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15210368-C-A

90695807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15209520-T-C

90695807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15209520-T-G

90695820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15209512-T-C

90695881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15209441-A-G

90695899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15209418-G-T

90695991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15209333-G-C

90696319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15209073-T-C

90696323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15209069-T-C

90696560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15208769-G-A

90696672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15208665-G-A

90696840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15208518-G-A

90697167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15208216-A-G

90697422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15207958-T-C

90697453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15207929-A-G

90697507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15207877-G-A

90697507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15207877-G-T

90697573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15207814-T-C

90700556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15205639-G-A

90701010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15205331-G-A

90701025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15205316-G-A

90701027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15205314-G-A

90701027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15205314-G-T

90701028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15205313-C-T

90701103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15205238-T-C

http://identifiers.org/hco/8/GRCh38#90701305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15205045-C-A

90701305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15205045-C-T

90701406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15204937-T-C

90701462-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15204880-A-T

90701515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15204820-T-C

90701546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15204782-C-T

90701626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15204708-T-C

http://identifiers.org/hco/8/GRCh38#90701643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#15204690-C-A

90701727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 15204607-T-C

90701727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 15204607-T-G

90701888-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15204454-T-A

90701894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15204448-C-T

90701908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15204435-A-G

90701927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15204417-T-C

90701959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15204385-G-A

90701959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15204385-G-T

90702002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15204332-A-G

90702076-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15204250-T-A

90702199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15204123-C-T

90702369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15203998-T-C

http://identifiers.org/hco/8/GRCh38#90702553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15203898-A-C

90703144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15203336-C-G

90703254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15203231-A-G

90703361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15203156-G-A

90703506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 15203028-T-C

http://identifiers.org/hco/8/GRCh38#90703522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15203012-C-A

90703522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 15203012-C-T

90703704-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15202827-T-G

http://identifiers.org/hco/8/GRCh38#90709791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15201438-C-A

90709816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15201413-T-C

90710826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15199511-A-G

90712872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15196776-T-C

90713328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15196172-G-A

90713328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15196172-G-T

90721191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15186371-G-A

90721321-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15186254-T-A

90721650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15185938-A-G

90721709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15185882-C-T

90755771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15177372-A-G

90755946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15177206-G-A

90756224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15176957-T-G

90756607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15176766-G-A

90756616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15176757-G-A

90756672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15176704-G-C

90757347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15175661-T-C

90757556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15175451-G-A

90757804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15175189-T-C

90757828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15175165-T-C

90758018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15174843-C-T

90758043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15174814-T-C

90758294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15174592-C-G

90758340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15174547-C-G

90758426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15173873-T-C

90758687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15173611-C-T

90758771-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15173530-T-G

90758858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15173445-T-G

http://identifiers.org/hco/8/GRCh38#90758971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15173322-C-A

90758973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15173320-T-C

90758998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15173205-A-G

90761933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15172562-C-T

90765522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15171395-A-G

90765540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15171379-T-C

90765615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15171288-A-G

90767817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15171704-A-G

90767817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15171704-A-T

90767848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15171681-T-C

90767988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15171550-G-A

http://identifiers.org/hco/8/GRCh38#90768047-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15171493-A-C

90768047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15171493-A-G

90768047-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15171493-A-T

90768134-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15171407-T-A

90768136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15171405-G-A

90768148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15171395-A-T

90768363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15171228-A-T

http://identifiers.org/hco/8/GRCh38#90769480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15170752-A-C

90769527-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15170698-T-G

90769703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15169141-G-A

90769705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15169139-G-A

90769736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15169108-T-C

90769843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15169000-T-C

90769862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15168981-A-G

90769927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15168936-A-T

90769969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15168900-A-G

90770224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15168644-C-T

90770263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15168564-G-A

90770621-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15167946-A-T

90770661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15167906-T-C

90770739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15167827-C-T

90770852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15167725-G-A

90770863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15167713-T-C

90771413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15167205-C-T

90771519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15167125-C-G

90771767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15166695-C-G

90771863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15166562-A-T

90771866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15166559-A-G

90771924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15166503-G-A

90771981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15166447-G-A

90772032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15166401-T-C

90772037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15166396-A-G

90772082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15166355-T-G

http://identifiers.org/hco/8/GRCh38#90772305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15166151-C-A

90772305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15166151-C-T

http://identifiers.org/hco/8/GRCh38#90772457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15166004-C-A

http://identifiers.org/hco/8/GRCh38#90772505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15165957-A-C

90779970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15162913-C-T

90780062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15162821-G-A

90780268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15162622-C-T

90780291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15162597-C-T

90780514-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15162397-T-A

90780514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15162397-T-C

90780514-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15162397-T-G

90780527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15162384-G-T

90780630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15162291-G-A

90780771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15162140-G-C

90780917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15162007-C-T

90780945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15161979-A-G

http://identifiers.org/hco/8/GRCh38#90781334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15161295-A-C

90781524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15161108-G-A

90781615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15161028-G-C

90781681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15160967-G-A

90781800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15160910-C-T

90781874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15160832-T-C

90781878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15160828-G-A

90781878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15160828-G-T

http://identifiers.org/hco/8/GRCh38#90781894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15160811-C-A

90785302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15159313-A-G

90785302-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15159313-A-T

90785357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15159256-A-G

90785497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15159159-T-G

90785533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15159122-C-T

90785617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15159046-T-C

90785674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15158989-T-C

90785689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15158974-G-A

http://identifiers.org/hco/8/GRCh38#90785722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15158940-C-A

90785959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15158720-T-C

90785962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15158717-A-G

90785973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15158706-A-G

90786124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15158561-A-G

http://identifiers.org/hco/8/GRCh38#90786141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15158545-C-A

90786399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15158320-A-G

90786404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15158315-C-T

90787068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15157018-A-G

90787309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15156771-T-C

90787447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15156632-G-A

90787635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15152620-C-T

90787943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15152330-G-T

90788364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15151896-G-A

http://identifiers.org/hco/8/GRCh38#90788365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15151895-A-C

http://identifiers.org/hco/8/GRCh38#90788903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15150568-C-A

90788927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15150544-G-A

90791537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 15149249-G-A

90791537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25441
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 15149249-G-T