39342457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28135710-G-A

39342457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28135710-G-C

39342457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28135710-G-T

39342507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28135660-G-A

39342507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28135660-G-C

39342507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28135660-G-T

39342538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28135599-G-A

39342538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28135599-G-T

39342591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28135546-G-A

39342591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28135546-G-T

http://identifiers.org/hco/19/GRCh38#39342594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#28135543-C-A

39342594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28135543-C-T

39343071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28135093-C-T

39343076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28135088-C-T

http://identifiers.org/hco/19/GRCh38#39343477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#28134737-A-C

39343477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28134737-A-G

39343517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28134698-G-C

39343581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28134650-G-C

39343702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28134557-G-T

39343741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28134523-C-T

39344123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28134233-G-A

http://identifiers.org/hco/19/GRCh38#39344282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#28134097-C-A

39344298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28134075-A-T

39344773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28133600-C-T

39345672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28132725-A-G

39345903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28132562-T-C

39346124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28132362-G-A

39346286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28132237-G-T

39346294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28132229-T-C

http://identifiers.org/hco/19/GRCh38#39346295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#28132228-C-A

39346295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28132228-C-T

39346584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28131889-A-G

39346681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28131792-A-G

39346934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28131659-G-A

39346961-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28131631-T-G

39347925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28130570-A-G

39347996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28130314-G-A

http://identifiers.org/hco/19/GRCh38#39348089-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#28130216-A-C

39349797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28128014-A-G

39349843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28127993-G-T

39349867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28127981-G-A

39349867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28127981-G-C

39349867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28127981-G-T

39350085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28127695-G-C

39350168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28127565-G-A

39350205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28127528-C-T

39351430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28126998-T-C

39351485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28126941-G-T

39351533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28126897-A-G

39351533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28126897-A-T

39351570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28126864-G-A

39351570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28126864-G-T

http://identifiers.org/hco/19/GRCh38#39351648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#28126796-C-A

39351938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28126613-G-A

39351973-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28126591-T-A

39352487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28124908-G-A

39352487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28124908-G-C

39352897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28124548-T-A

http://identifiers.org/hco/19/GRCh38#39356627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#28123322-C-A

http://identifiers.org/hco/19/GRCh38#39356648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#28123301-A-C

39356648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28123301-A-G

39356648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28123301-A-T

http://identifiers.org/hco/19/GRCh38#39356650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#28123299-C-A

39356650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28123299-C-T

http://identifiers.org/hco/19/GRCh38#39356651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#28123298-C-A

http://identifiers.org/hco/19/GRCh38#39356717-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#28123232-A-C

39356717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28123232-A-G

39356717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28123232-A-T

39357181-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28122772-T-A

39357458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28122572-G-A

39357774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28122277-G-A

39358723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28121898-A-G

39358767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28121852-A-G

39358972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28121670-C-T

39358980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28121662-C-T

39359221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28121419-C-T

39359453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28121229-A-G

39359711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28120831-G-A

39360216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28120450-A-G

39360277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28120396-G-T

39360619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28120069-G-A

39360759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28119937-C-T

39360828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28119873-A-G

http://identifiers.org/hco/19/GRCh38#39360844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#28119840-C-A

39362625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28119298-A-G

39362631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28119292-A-G

39362689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28119244-G-A

http://identifiers.org/hco/19/GRCh38#39362706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#28119227-C-A

39362706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28119227-C-G

39362728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28119209-A-G

39362772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28119172-C-G

39362772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28119172-C-T

39362918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28119022-C-T

39363119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28118838-G-A

39363826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28118102-C-T

http://identifiers.org/hco/19/GRCh38#39363931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#28118000-C-A

39364096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28117835-A-G

39364166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28117765-C-T

39365812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28116721-G-T

39366702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28116391-G-A

39366702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28116391-G-T

39366902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28116152-C-T

39366923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28116132-G-C

39367105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28115950-T-C

39368466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28114986-A-G

39368930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28114245-A-G

http://identifiers.org/hco/19/GRCh38#39369151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#28114049-C-A

39369151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28114049-C-T

39369167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28114034-A-G

http://identifiers.org/hco/19/GRCh38#39369171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#28114030-C-A

39369194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28114004-G-A

39369194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28114004-G-T

39369281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28113969-T-C

39369281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28113969-T-G

39369423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28113961-G-T

39369437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28113947-G-C

http://identifiers.org/hco/19/GRCh38#39369442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#28113942-C-A

39369442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28113942-C-T

39369446-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28113938-T-G

39369479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28113921-G-A

39369479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28113921-G-T

39369480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28113920-G-T

39369484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28113916-G-T

39369551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28113859-A-G

39369551-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28113859-A-T

http://identifiers.org/hco/19/GRCh38#39369566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#28113844-C-A

39369566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28113844-C-T

39369575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28113836-T-C

39369878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 28113542-C-T

39370050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28113370-A-G

http://identifiers.org/hco/19/GRCh38#39370069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#28113351-A-C

http://identifiers.org/hco/19/GRCh38#39370086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#28113334-C-A

39370086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28113334-C-T

http://identifiers.org/hco/19/GRCh38#39370089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#28113331-C-A

39370205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28113229-G-A

39370302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28113129-A-G

39370312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28113120-T-C

39370666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28112117-T-C

39370874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28111941-T-C

39371439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28111600-G-A

39371439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28111600-G-T

39371463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28111577-T-C

39372212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28111102-T-C

39373280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28110102-G-A

http://identifiers.org/hco/19/GRCh38#39375706-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#28107542-A-C

39375706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28107542-A-G

39375919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28107330-T-C

39375937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28107312-A-G

39376612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28106827-A-G

39377031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28106428-C-T

39377078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28106408-T-C

39377124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28106367-A-G

39377335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28106214-G-A

39377335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28106214-G-C

39377335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28106214-G-T

39377507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28106088-T-C

http://identifiers.org/hco/19/GRCh38#39377530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#28106065-C-A

39377715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28105901-G-C

39377860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28105760-G-T

39377867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28105753-G-T

39377870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28105750-A-G

http://identifiers.org/hco/19/GRCh38#39377953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#28105669-A-C

39377953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28105669-A-G

39377975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28105646-T-A

39377975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28105646-T-C

39380505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28103555-G-T

http://identifiers.org/hco/19/GRCh38#39380714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#28103358-C-A

39380871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28103219-T-C

http://identifiers.org/hco/19/GRCh38#39381147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#28103002-C-A

39381147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28103002-C-T

39381181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28102968-G-T

39381205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28102947-G-C

39381205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28102947-G-T

http://identifiers.org/hco/19/GRCh38#39381210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#28102942-C-A

39381210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28102942-C-T

39381267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28102886-G-T

39381288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28102867-T-C

39381288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28102867-T-G

http://identifiers.org/hco/19/GRCh38#39381337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#28102826-C-A

39381337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28102826-C-T

http://identifiers.org/hco/19/GRCh38#39381347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#28102816-A-C

39381347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28102816-A-G

39381347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28102816-A-T

http://identifiers.org/hco/19/GRCh38#39381354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#28102809-C-A

39381354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28102809-C-T

39381461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28102714-G-A

39381585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28102598-G-C

39382363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28102109-A-G

39382363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28102109-A-T

39382560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28101945-C-T

39382785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28101766-G-A

39382894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28101673-C-T

39383077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28101468-T-A

39383747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28100796-G-A

39383747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28100796-G-T

39383902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28100654-C-G

39383902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28100654-C-T

39384073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28100517-A-G

http://identifiers.org/hco/19/GRCh38#39384332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#28100268-C-A

39384343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28100258-G-A

39384414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28100186-T-G

39384489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28100113-G-T

39384537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28100073-A-G

39385061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28099555-G-A

39385061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28099555-G-T

39385327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28099294-T-A

39385327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28099294-T-C

39385617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28099025-G-A

http://identifiers.org/hco/19/GRCh38#39385789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#28098866-C-A

39385789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28098866-C-T

http://identifiers.org/hco/19/GRCh38#39385791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#28098864-C-A

39385791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28098864-C-G

39385791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28098864-C-T

39385797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28098858-G-A

39385797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28098858-G-T

39386133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28098519-C-T

39386606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28098048-G-C

39386828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28097843-G-A

39388203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28096677-C-T

39390524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25492
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant, undefined
orthologous variants: 28092883-A-G