http://identifiers.org/hco/1/GRCh38#19484512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
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/4/GRCm39#138921220-C-A

19484512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 138921220-C-G

19484512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 138921220-C-T

19484539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 138921194-G-A

http://identifiers.org/hco/1/GRCh38#19484623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
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/4/GRCm39#138921090-C-A

19484623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 138921090-C-T

19484723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 138920985-G-A

19484723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 138920985-G-T

19484737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 138920977-G-A

19484737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 138920977-G-T

19484769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 138920947-G-C

19484769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 138920947-G-T

http://identifiers.org/hco/1/GRCh38#19484801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#138920916-C-A

19484801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 138920916-C-G

19484801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 138920916-C-T

19484837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 138920876-G-A

19484837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 138920876-G-C

19485031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138920700-G-A

19485031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138920700-G-C

19485179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138920574-A-G

19485187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138920566-G-A

http://identifiers.org/hco/1/GRCh38#19485350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#138920428-C-A

19485350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138920428-C-G

19485350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138920428-C-T

19485392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138920386-C-T

19485394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138920384-G-A

19485394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138920384-G-C

19485394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138920384-G-T

19485403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138920375-C-G

19485403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138920375-C-T

19485584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138920178-T-A

19485584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138920178-T-C

19485608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138920156-G-A

19485608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138920156-G-T

19486168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138919712-A-G

19486937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138919160-G-C

19486972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138919126-G-A

http://identifiers.org/hco/1/GRCh38#19493990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138909615-C-A

19493990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138909615-C-T

19495986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138907989-T-A

19495991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138907984-G-A

19496100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138907879-C-T

19496356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138907624-T-C

http://identifiers.org/hco/1/GRCh38#19496778-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138907187-A-C

19496911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138907059-T-A

19499867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138905262-T-C

http://identifiers.org/hco/1/GRCh38#19504858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138903802-C-A

19504858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138903802-C-G

19505311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138903370-T-C

http://identifiers.org/hco/1/GRCh38#19505343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138903338-A-C

19505390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138903265-G-A

19505390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138903265-G-T

19505856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138902824-C-T

19505900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138902780-G-A

19506170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138902599-C-T

19506268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138902516-A-G

19506268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138902516-A-T

19506279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138902505-A-G

19513615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138898531-C-T

http://identifiers.org/hco/1/GRCh38#19513694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138898454-A-C

19513694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138898454-A-G

19513699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138898449-C-T

19514728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138898055-C-T

19514979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138897791-A-G

http://identifiers.org/hco/1/GRCh38#19514980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138897790-C-A

19514980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138897790-C-T

19514981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138897789-A-G

http://identifiers.org/hco/1/GRCh38#19517521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138896657-C-A

19529729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138894645-C-T

19529733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138894641-G-A

19529823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138894553-G-A

19529869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138894506-C-G

http://identifiers.org/hco/1/GRCh38#19529992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138894386-C-A

19532488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138892797-C-T

19532580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138892728-T-C

19532717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138892589-G-A

19532728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138892578-C-T

19532785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138892515-G-A

19533691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138892213-G-A

19533800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138892102-G-C

19533916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138892066-G-A

19533957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138892026-T-C

19534158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138891858-A-G

19534158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138891858-A-T

19534165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138891851-G-A

19534425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138891597-G-A

19534514-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138891541-T-A

19534603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138891419-T-C

http://identifiers.org/hco/1/GRCh38#19534658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138891367-A-C

19534717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138891313-A-T

http://identifiers.org/hco/1/GRCh38#19563039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138882713-C-A

19563356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138882572-A-G

19563356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138882572-A-T

19563710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138882234-A-G

19563715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138882229-G-A

19563723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138882221-G-A

19563845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138882113-A-G

19563959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138882002-C-T

19563982-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138881979-T-G

19564094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138881869-G-A

19564121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138881842-G-A

19564121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138881842-G-C

http://identifiers.org/hco/1/GRCh38#19564348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138881608-C-A

19564348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138881608-C-G

19577248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138874156-A-G

19577992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138872229-G-A

19582489-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138867722-T-A

19582559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138867566-C-T

19591342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138866321-A-G

http://identifiers.org/hco/1/GRCh38#19591368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138866298-C-A

19591368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138866298-C-G

19591368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138866298-C-T

19591369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron variant
orthologous variants: 138866297-T-C

19591827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 138866191-G-T

19591966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138866053-T-C

19596882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, undefined
orthologous variants: 138858458-A-G

http://identifiers.org/hco/1/GRCh38#19596901-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#138858437-A-C

19596901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, undefined
orthologous variants: 138858437-A-G

http://identifiers.org/hco/1/GRCh38#19596996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#138858344-C-A

19596996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 138858344-C-G

19596996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 138858344-C-T

19597009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 138858331-C-G

19597009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 138858331-C-T

19597064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 138858276-G-A

19597064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 138858276-G-C

19597094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 138858246-G-A

http://identifiers.org/hco/1/GRCh38#19597229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#138858136-C-A

19597229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138858136-C-T

19597291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138858056-A-G

19597327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138858021-G-T

19597496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138857877-C-T

http://identifiers.org/hco/1/GRCh38#19597780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#138857599-A-C

http://identifiers.org/hco/1/GRCh38#19597782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#138857597-C-A

http://identifiers.org/hco/1/GRCh38#19597851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138857491-C-A

19597901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138857438-G-T

19598112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138856667-T-A

19598112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138856667-T-C

19598123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138856656-T-C

19600277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138854571-A-T

19601656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138853689-T-C

19601849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138853533-T-A

19602198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138853186-A-G

19602292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138853088-A-G

19602446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138852442-G-A

19602705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138852217-T-A

19604805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138851588-T-A

19607201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138848077-G-A

http://identifiers.org/hco/1/GRCh38#19607242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138848037-A-C

19610772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138845418-T-C

19614679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138842991-T-C

19614828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138842879-A-G

19616838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138842731-G-A

19617181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138842444-A-G

19617286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138842350-A-G

19617291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138842345-C-T

19617293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138842343-G-T

19617298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138842338-T-C

19617340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138842328-A-G

http://identifiers.org/hco/1/GRCh38#19617360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138842309-C-A

19617360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138842309-C-T

19617442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138842231-G-T

19617752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138841914-C-T

19617862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138841818-A-G

http://identifiers.org/hco/1/GRCh38#19618531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138841439-C-A

19619718-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138839202-T-A

19619750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138839170-G-A

19619821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138839101-G-T

http://identifiers.org/hco/1/GRCh38#19620531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138838446-A-C

19621351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138837724-A-G

19621352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138837723-T-C

19621478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138837602-C-T

19621634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138833616-G-A

19621766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138833528-G-A

19621994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138833318-T-A

19621994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138833318-T-C

19622031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138833287-G-T

19622046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138833271-T-A

19622046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138833271-T-C

19622434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138832969-T-C

19623464-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138832417-T-G

19623588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138832294-G-A

http://identifiers.org/hco/1/GRCh38#19623591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138832291-C-A

19623591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 138832291-C-T

http://identifiers.org/hco/1/GRCh38#19623686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138832203-C-A

19623693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138832196-G-A

19623693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138832196-G-C

19623693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138832196-G-T

19625676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138831933-A-G

19625727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138831885-G-A

http://identifiers.org/hco/1/GRCh38#19625772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138831841-C-A

19625772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138831841-C-G

19626179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138831478-C-T

19626708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 138831034-A-G

19627751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 138830565-G-C

19627751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 138830565-G-T

http://identifiers.org/hco/1/GRCh38#19629004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138829961-C-A

19629004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 138829961-C-T

19629034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 138829931-T-C

19629222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 138829736-C-T

19629354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 138829603-G-A

19629354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 138829603-G-T

19629816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32068
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 138829143-C-T