http://identifiers.org/hco/7/GRCh38#149838407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#48481272-C-A

149838407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 48481272-C-G

149838409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 48481274-A-G

149838421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 48481285-G-T

149838423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 48481287-G-A

149838423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 48481287-G-T

149838458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 48481320-C-G

149838458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 48481320-C-T

149838513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48481371-C-T

http://identifiers.org/hco/7/GRCh38#149838552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#48481403-C-A

149838552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48481403-C-G

149838552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48481403-C-T

149838564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48481415-G-A

149838564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48481415-G-T

http://identifiers.org/hco/7/GRCh38#149838565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#48481416-C-A

149838565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48481416-C-T

http://identifiers.org/hco/7/GRCh38#149838566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#48481417-C-A

149838566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48481417-C-T

http://identifiers.org/hco/7/GRCh38#149838567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#48481418-A-C

149838567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48481418-A-G

149838585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48481436-G-A

149838585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48481436-G-T

149838606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48481455-G-A

149838606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48481455-G-T

http://identifiers.org/hco/7/GRCh38#149838667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48481513-C-A

149838667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48481513-C-T

149838732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48481548-T-C

149838770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48481586-T-C

http://identifiers.org/hco/7/GRCh38#149838771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#48481587-C-A

149838771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48481587-C-G

149838771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48481587-C-T

http://identifiers.org/hco/7/GRCh38#149838776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#48481604-C-A

149838776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48481604-C-G

149838776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48481604-C-T

http://identifiers.org/hco/7/GRCh38#149838869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48481666-C-A

149839003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48481812-G-T

149839237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48482077-C-G

149839422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48482367-A-G

http://identifiers.org/hco/7/GRCh38#149839439-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48482384-A-C

149839586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48482549-C-T

149839594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48482557-A-G

149839666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48482616-A-G

149839839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48482838-C-T

149839972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48482936-T-C

149842467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48483470-A-G

149844413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48484990-C-T

149844503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48485079-G-A

149844503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48485079-G-T

149844645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 48485226-C-T

149844801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48485381-G-A

149844801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48485381-G-T

http://identifiers.org/hco/7/GRCh38#149844922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48485463-C-A

http://identifiers.org/hco/7/GRCh38#149844935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48485473-A-C

http://identifiers.org/hco/7/GRCh38#149844941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48485479-C-A

149844970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48485509-G-A

149844970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48485509-G-T

http://identifiers.org/hco/7/GRCh38#149845003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48485548-C-A

149845003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48485548-C-T

149845187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48485852-T-A

149845187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48485852-T-C

149845187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48485852-T-G

149845198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48485862-T-G

149845240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48485960-G-A

149845240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48485960-G-T

149845367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48486194-G-A

149845394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48486221-G-A

149845395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48486222-C-T

149845481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48486300-G-C

149845481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48486300-G-T

149845552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48486373-T-C

http://identifiers.org/hco/7/GRCh38#149845762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48486584-C-A

149845763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48486585-C-T

149845815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48486674-C-T

149845938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48486823-T-C

149845938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48486823-T-G

149846055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48486932-G-T

149846058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48486935-G-A

149846058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48486935-G-T

149846092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48486973-G-A

149846092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48486973-G-T

http://identifiers.org/hco/7/GRCh38#149846093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48486974-C-A

http://identifiers.org/hco/7/GRCh38#149846094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48486975-C-A

149846094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48486975-C-G

149846094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48486975-C-T

149846110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48486989-T-C

http://identifiers.org/hco/7/GRCh38#149846154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48487013-C-A

149846154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 48487013-C-T

http://identifiers.org/hco/7/GRCh38#149846157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48487016-C-A

149846168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 48487027-C-G

149846180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 48487039-C-T

149846222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, stop_gained
orthologous variants: 48487081-C-T

149846245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 48487104-G-A

149846245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 48487104-G-C

http://identifiers.org/hco/7/GRCh38#149846272-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48487130-A-C

149846284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48487141-A-G

http://identifiers.org/hco/7/GRCh38#149846311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48487170-A-C

149846311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48487170-A-G

http://identifiers.org/hco/7/GRCh38#149846350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48487204-C-A

149846350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48487204-C-G

149846350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48487204-C-T

http://identifiers.org/hco/7/GRCh38#149846375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48487234-C-A

149846375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48487234-C-T

http://identifiers.org/hco/7/GRCh38#149846379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48487238-C-A

149846385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48487244-G-A

149846385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48487244-G-T

http://identifiers.org/hco/7/GRCh38#149846592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48487429-C-A

149846622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48487459-G-A

149846728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48487499-T-C

149846865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48487635-C-T

149847051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48487794-T-C

149847140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48487880-A-G

http://identifiers.org/hco/7/GRCh38#149847152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48487892-A-C

149847205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48487956-A-G

149847363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48488422-C-G

149847557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48488627-G-A

149847592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48488661-G-A

149847592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48488661-G-T

149847648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48488673-T-G

149847742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 48488756-A-T

149847771-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense variant
orthologous variants: 48488785-T-G

149847801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense variant
orthologous variants: 48488815-C-T

http://identifiers.org/hco/7/GRCh38#149847859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48488872-C-A

149847859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense variant
orthologous variants: 48488872-C-G

149847859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: synonymous variant
orthologous variants: 48488872-C-T

http://identifiers.org/hco/7/GRCh38#149847893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48488907-C-A

149847893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: synonymous variant
orthologous variants: 48488907-C-T

149847937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: synonymous variant
orthologous variants: 48488951-G-A

http://identifiers.org/hco/7/GRCh38#149847946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48488960-C-A

149847946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense variant
orthologous variants: 48488960-C-G

149848020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense variant
orthologous variants: 48489034-G-T

149848027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense variant
orthologous variants: 48489041-A-G

149848041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense variant
orthologous variants: 48489055-G-A

149848041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense variant
orthologous variants: 48489055-G-T

149848114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: synonymous variant
orthologous variants: 48489128-A-G

149848129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 48489143-C-T

149848136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48489150-G-C

http://identifiers.org/hco/7/GRCh38#149848341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/6/GRCm39#48489355-C-A

149848341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 48489355-C-G

149848342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 48489356-A-G

http://identifiers.org/hco/7/GRCh38#149848439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48489453-C-A

149848439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48489453-C-G

149848439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48489453-C-T

149848461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48489473-T-A

149849003-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48490104-A-T

http://identifiers.org/hco/7/GRCh38#149849340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48490379-C-A

149849478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48490481-A-G

149849629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48490611-G-C

149849744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48490730-T-G

149849771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48490758-A-G

149849861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48490837-C-T

149850030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48490982-A-T

149850308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48491230-C-T

149850362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48491284-T-A

http://identifiers.org/hco/7/GRCh38#149850367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48491289-C-A

149850367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48491289-C-T

http://identifiers.org/hco/7/GRCh38#149850467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48491372-C-A

149850467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48491372-C-G

149850472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48491377-G-A

149850472-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48491377-G-C

149850472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48491377-G-T

149850477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48491382-T-C

http://identifiers.org/hco/7/GRCh38#149850482-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48491387-A-C

149850482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48491387-A-T

http://identifiers.org/hco/7/GRCh38#149850531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48491437-C-A

149850531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48491437-C-T

http://identifiers.org/hco/7/GRCh38#149850570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48491480-C-A

http://identifiers.org/hco/7/GRCh38#149850601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48491509-C-A

149850601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48491509-C-T

149850718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48491586-C-G

149850718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48491586-C-T

149850751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48491623-G-A

149850751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48491623-G-T

149850784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48491657-A-G

149850784-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48491657-A-T

149850831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48491696-G-A

149850831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48491696-G-T

149850850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48491719-G-A

149850903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48491795-G-A

149850903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48491795-G-T

149850942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48491811-G-A

149850942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48491811-G-T

149850956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48491825-G-T

149850978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48491847-G-C

http://identifiers.org/hco/7/GRCh38#149850992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48491861-C-A

149850992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48491861-C-T

149851093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48491941-G-A

149852734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48495215-G-T

149855931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48495864-A-G

149855994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48495933-A-G

http://identifiers.org/hco/7/GRCh38#149855999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48495938-C-A

149855999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48495938-C-T

149856011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48495949-T-C

149856030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48495968-G-A

149856030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48495968-G-T

http://identifiers.org/hco/7/GRCh38#149856044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#48495982-C-A

149856044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 48495982-C-G

149856044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 48495982-C-T

http://identifiers.org/hco/7/GRCh38#149856047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#48495985-C-A

149856057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48495995-A-G

149857863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48503002-G-A

149857869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48503008-T-C

149858017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48503139-T-C

http://identifiers.org/hco/7/GRCh38#149858173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48503294-C-A

http://identifiers.org/hco/7/GRCh38#149858303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48503375-C-A

149858305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48503378-T-C

149858342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48503406-C-T

149858451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48503508-C-T

149858466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48503518-A-G

http://identifiers.org/hco/7/GRCh38#149858542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48503568-C-A

149858542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48503568-C-T

http://identifiers.org/hco/7/GRCh38#149858545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48503571-C-A

149858545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48503571-C-T

http://identifiers.org/hco/7/GRCh38#149859026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48503980-A-C

149859026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48503980-A-G

149859071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504020-G-A

149859071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504020-G-T

149859099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504047-C-T

149859100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504048-A-G

149859143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504094-T-C

http://identifiers.org/hco/7/GRCh38#149859169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48504113-C-A

149859169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504113-C-T

149859181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504136-T-C

149859194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504160-G-A

149859194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504160-G-C

149859194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504160-G-T

149859205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504170-G-A

149859205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504170-G-T

http://identifiers.org/hco/7/GRCh38#149859279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48504250-C-A

149859279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504250-C-T

149859301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504269-A-G

149859301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504269-A-T

149859305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504273-T-C

149859324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504289-G-A

149859324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504289-G-C

149859324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504289-G-T

149859383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504343-C-G

http://identifiers.org/hco/7/GRCh38#149859473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48504430-C-A

149859473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48504430-C-T

http://identifiers.org/hco/7/GRCh38#149859569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48504526-C-A

http://identifiers.org/hco/7/GRCh38#149859604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48504561-C-A

149859604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504561-C-T

http://identifiers.org/hco/7/GRCh38#149859607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48504564-C-A

149859607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504564-C-T

149859635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504588-G-A

149859635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504588-G-C

149859635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504588-G-T

149859734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504666-T-C

149859833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504757-T-C

http://identifiers.org/hco/7/GRCh38#149859885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48504807-A-C

149859885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504807-A-G

149859889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504811-G-A

149859894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504816-T-C

149859909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504831-T-A

149859909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504831-T-C

149859923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504843-C-T

149859925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504845-G-A

149859925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504845-G-T

149859979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504898-G-T

149860011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504927-A-G

149860011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504927-A-T

http://identifiers.org/hco/7/GRCh38#149860066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48504975-C-A

149860066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504975-C-G

149860066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48504975-C-T

149860097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48505007-G-T

http://identifiers.org/hco/7/GRCh38#149860108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48505018-C-A

149860108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48505018-C-T

http://identifiers.org/hco/7/GRCh38#149860110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48505020-C-A

149860110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48505020-C-T

149860155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48505061-T-C

149860156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48505062-G-T

149860186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48505092-T-C

149860193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48505099-G-A

149860193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48505099-G-T

149860335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48505238-G-T

149860339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48505242-A-T

149860340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48505243-G-A

149860382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 48505284-G-A

149860401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48505303-C-T

149860421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 48505329-C-T

149860441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 48505349-C-T

149860479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48505384-C-T

149860547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48505455-C-T

http://identifiers.org/hco/7/GRCh38#149860660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48505568-A-C

149860660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 48505568-A-G

149860664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48505572-C-G

149860664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48505572-C-T

149860685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48505593-G-A

149860754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48505662-G-A

149860775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48505683-C-T

149860838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48505746-A-G

149860951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 48505848-G-A

149860951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 48505848-G-T

149861005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 48505902-G-A

149861012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48505909-G-A

149861015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48505912-C-T

149861054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48505951-A-G

149861062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 48505959-C-T

149861066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48505963-G-A

149861066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 48505963-G-T

http://identifiers.org/hco/7/GRCh38#149861090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48505987-A-C

149861129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48506026-A-G

149861136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48506033-T-C

http://identifiers.org/hco/7/GRCh38#149861139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48506036-C-A

149861139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48506036-C-G

149861139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48506036-C-T

149861159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48506056-G-A

http://identifiers.org/hco/7/GRCh38#149861179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48506075-C-A

149861179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 48506075-C-T

149861184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48506080-T-A

149861342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 48506238-C-T

149861350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 48506246-C-T

149861372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 48506268-G-A

149861402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 48506298-C-G

149861402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 48506298-C-T

149861555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 48506451-G-A

149861557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 48506453-G-A

149861557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 48506453-G-T

149861590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 48506470-C-T

149861725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 48506605-C-T

149861780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 48506660-C-T

149861789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 48506669-G-A

149861789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 48506669-G-T

http://identifiers.org/hco/7/GRCh38#149861826-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48506706-A-C

http://identifiers.org/hco/7/GRCh38#149861869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48506749-C-A

149861869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 48506749-C-T

149861897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48506777-G-C

http://identifiers.org/hco/7/GRCh38#149861906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48506786-C-A

149861906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48506786-C-G

149861906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48506786-C-T

149861979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48506859-G-A

149861979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48506859-G-T

149862019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48506899-G-A

149862038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48506918-G-A

149862038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48506918-G-C

149862061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 48506941-T-C

149862070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 48506950-C-T

149862088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48506968-C-G

149862088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 48506968-C-T

149862089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48506969-G-A

http://identifiers.org/hco/7/GRCh38#149862090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48506970-A-C

149862091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 48506971-G-A

149862091-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48506971-G-C

149862122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48507002-G-C

149862134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 48507014-G-T

http://identifiers.org/hco/7/GRCh38#149862179-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48507059-A-C

149862212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48507092-C-G

149862212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48507092-C-T

149862240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48507120-C-T

149862265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 48507145-C-T

149862281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48507161-C-T

149862303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48507183-G-A

149862303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48507183-G-T

149862312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48507192-C-T

149862329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48507209-C-T

http://identifiers.org/hco/7/GRCh38#149862440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48507320-C-A

149862440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48507320-C-T

149862441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48507321-G-A

149862444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48507324-G-A

http://identifiers.org/hco/7/GRCh38#149862471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48507351-A-C

149862471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48507351-A-G

149862483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48507363-G-A

http://identifiers.org/hco/7/GRCh38#149862556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48507461-C-A

149862556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48507461-C-T

149862563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48507468-G-A

149862563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48507468-G-T

149862589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48507500-G-A

149862589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48507500-G-T

149862610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48507526-C-T

149862616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48507534-G-A

149862616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48507534-G-C

149862623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48507541-A-G

149862898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48507905-G-T

149862995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48508007-C-G

149863235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48508221-A-G

149863376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48508300-C-T

149863558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48508461-G-C

149863568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48508471-C-G

149863620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48508517-C-G

149863681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48508584-C-T

149863823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48508708-A-G

149863929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48508811-C-G

149863981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48508863-A-G

149863981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48508863-A-T

149864040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48508907-G-A

149864040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48508907-G-T

149864047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48508914-G-T

149864061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48508925-G-A

149864061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48508925-G-T

http://identifiers.org/hco/7/GRCh38#149864091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48508951-C-A

149864091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48508951-C-T

http://identifiers.org/hco/7/GRCh38#149864098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48508958-C-A

149864098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48508958-C-G

149864098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron variant
orthologous variants: 48508958-C-T

http://identifiers.org/hco/7/GRCh38#149864101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48508961-C-A

149864101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 48508961-C-G

149864101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 48508961-C-T

http://identifiers.org/hco/7/GRCh38#149864156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48509016-C-A

149864156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense variant
orthologous variants: 48509016-C-T

http://identifiers.org/hco/7/GRCh38#149864171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48509031-C-A

149864171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense variant
orthologous variants: 48509031-C-T

149864244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense variant
orthologous variants: 48509090-T-A

http://identifiers.org/hco/7/GRCh38#149864270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48509115-C-A

149864270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: missense variant
orthologous variants: 48509115-C-T

http://identifiers.org/hco/7/GRCh38#149864272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48509117-C-A

149864272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: synonymous variant
orthologous variants: 48509117-C-G

149864272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: synonymous variant
orthologous variants: 48509117-C-T

149864312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48509152-G-T

149864315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48509155-G-A

149864315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48509155-G-C

149864404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48509228-A-G

149864485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48509293-G-A

149864485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48509293-G-T

http://identifiers.org/hco/7/GRCh38#149864522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48509331-C-A

149864522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48509331-C-T

http://identifiers.org/hco/7/GRCh38#149864530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48509339-C-A

149864530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48509339-C-T

http://identifiers.org/hco/7/GRCh38#149864557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48509356-C-A

http://identifiers.org/hco/7/GRCh38#149864567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48509366-A-C

149864567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48509366-A-G

149864676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48509467-T-C

149864676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48509467-T-G

149864700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48509486-G-A

149864700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48509486-G-C

149864726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48509510-G-A

149864726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48509510-G-T

149864735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48509519-G-A

149864735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48509519-G-T

http://identifiers.org/hco/7/GRCh38#149864736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48509520-C-A

149864736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48509520-C-T

149864737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48509521-T-A

149864737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48509521-T-C

149864759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48509547-G-T

149864794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48509567-A-G

http://identifiers.org/hco/7/GRCh38#149864852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48509604-C-A

149864852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48509604-C-T

149864980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48509721-G-A

149864980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48509721-G-T

http://identifiers.org/hco/7/GRCh38#149865013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48509762-A-C

http://identifiers.org/hco/7/GRCh38#149865019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48509769-C-A

149865019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48509769-C-G

149865019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48509769-C-T

149865033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48509782-G-T

149865255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 48509996-G-A

149865255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 48509996-G-T

http://identifiers.org/hco/7/GRCh38#149865314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48510048-C-A

149865332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 48510066-G-A

149865332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 48510066-G-T

http://identifiers.org/hco/7/GRCh38#149865335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#48510069-C-A

149865335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 48510069-C-T

149865394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48510150-A-G

149865436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48510190-C-G

149865468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48510222-G-T

149865494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48510238-C-T

149865545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48510287-T-C

149865580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48510321-G-T

http://identifiers.org/hco/7/GRCh38#149865699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48510430-C-A

http://identifiers.org/hco/7/GRCh38#149865708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48510439-C-A

149865766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48510478-C-T

149865924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48510540-C-T

149866075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48510581-G-C

149866075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48510581-G-T

149866129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48510616-T-C

http://identifiers.org/hco/7/GRCh38#149866194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48510657-C-A

149866329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48510741-G-T

149866467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48510827-C-T

149866490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48510848-G-T

149866644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48510984-A-G

149866708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48511048-T-C

http://identifiers.org/hco/7/GRCh38#149866737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48511057-C-A

149866737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48511057-C-T

149867004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48511331-G-A

149867004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48511331-G-T

149867047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48511377-A-G

149867275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48511567-A-G

http://identifiers.org/hco/7/GRCh38#149867326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#48511619-C-A

149867339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48511632-G-A

149867339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48511632-G-T

149867408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34519
most severe consequence: 3 prime UTR variant
orthologous variants: 48511698-A-G